Zoll E Service manual

SERVICE MANUAL
ZOLL MEDICAL CORPORATION
9650-1450-01 Rev. A October 2008
ZOLL, E Series, and RescueNet are registered trademarks, and SurePower Charger Station is a trademark of ZOLL Medical Corporation. All other trademarks and registered trademarks are property of their respective owners.
Copyright © 2008 ZOLL Medical Corporation. All rights reserved.
9650-1450-01 Rev. A
TABLE OF CONTENTS
Preface .............................................................................................................................................................. v
Safety Considerations......................................................................................................................... ... .... ... ... ... .... ... . v
Additional Reference Material ........................................ .... ... ... ................................................................................. vi
Conventions................................................................................................................................................................ vi
Service Policy Warranty............................................................................................................................................ vii
Technical Service.................................... ... ... ... .... ... ................................................ ... .... ............................................ vii
Technical Service for International Customers ..................................................................................................... vi ii
Ch a p t e r 1 Maintenance Tests ........................................................................................................................ 1-1
Overview.................................................................................................................................................................... 1-1
Before You Begin the Maintenance Tests............................................................................................................... 1-2
Equipment You Need to Perform the Maintenance Tests...................................................................................... 1-2
Equipment You Need for the E Series Options Maintenance Tests ..................................................................... 1-3
Physical Inspection of the Unit............................................................................................................................. 1-4
Front Panel Button Test....................................................................................................................................... 1-6
3, 5, and 12 Leads Test....................................................................................................................................... 1-9
Power Supply Test (Optional)............................................................................................................................ 1-10
Leakage Current Test........................................................................................................................................ 1-14
Paddles Test (If applicable)............................................................................................................................... 1-15
Heart Rate Display Test..................................................................................................................................... 1-16
Calibrating Pulses on Strip Chart Test............................................................................................................... 1-17
Notch Filter Test ................................................................................................................................................ 1-18
Heart Rate Alarm Test....................................................................................................................................... 1-19
Defibrillator Self Test ......................................................................................................................................... 1-21
Synchronized Cardioversion Test...................................................................................................................... 1-23
Shock Test......................................................................................................................................................... 1-24
Summary Report Test........................................................................................................................................ 1-26
Advisory Message Test ..................................................................................................................................... 1-27
Pacer Test ......................................................................................................................................................... 1-28
SpO2 Monitor Test for SpO2 Option.................................................................................................................. 1-31
EtCO2 Monitor Test (for EtCO2 Option)............................................................................................................ 1-33
Barometric Pressure Calibration Check.............................................................................................................. 1-34
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CO2 Accuracy Check .......................... ... ... ... .... ... ... ... ................................................. ... ... ... ............................... 1-35
NIBP Monitor Test .............................................................................................................................................. 1-37
NIBP Volume Leak Test with Bio-Tek NIBP Analyzer........................................................................................ 1-39
NIBP Volume Leak Test with Fluke Biomedical Cufflink NIBP Analyzer....................................................... ... .. 1-41
NIBP Transducer Calibration Test...................................................................................................................... 1-43
Ch a p t e r 2 Troubleshooting ............................................................................................................................... 2-1
Overview.................................................................................................................................................................... 2-1
Troubleshooting........................................................................................................................................................ 2-2
ZOLL E Series Error Messages ............................................................................................................................... 2-5
Ch a p t e r 3 Replacement Parts........................................................................................................................... 3-1
Replacement Parts.................................................................................................................................................... 3-2
Field Replacement Parts.......................................................................................................................................... 3-5
Ch a p t e r 4 Functional Description.................................................................................................................... 4-1
Main System Board............................. .... ................................................ ... ... .... ... ... ... .... ... ........................................ 4-2
Main System Board Functions ............................................................................................................................... 4-4
Power Supply ......................................................................................................................................................... 4-5
ECG Front End ...................................................................................................................................................... 4-6
Multifunction Electrode (MFE)/PADS (System Board and High Voltage Module) ................................................. 4-6
CPU and EPU ........................................................................................................................................................ 4-6
High Voltage Module................................................................................................................................................. 4-7
Defibrillator Charging and Discharging ......... .... ..................................................................................................... 4-7
Charging .................................................................................................................................................. 4-7
Discharging .................................. .......................................... .................................................................. 4-8
High Voltage Capacitor Monitor ............................................................................................................................. 4-8
Pacer/Defibrillator Control Signals ......................................................................................................................... 4-9
Internal Discharge Resistor Module ..................................................................................................................... 4-10
AC/DC Charger Module.......................................................................................................................................... 4-10
System Interconnect Module..................................................................................................................................4-11
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Stripchart Recorder .............................................................................................................................................. 4-11
PCMCIA Slots ...................................................................................................................................................... 4-11
Front Panel and Controls PWBA ......................................................................................................................... 4-11
Isolated Power Supply Module ......................... ... ... ... ... .... ... ... ... .... ...................................................................... 4-11
E Series Options..................................................................................................................................................... 4-12
12 Lead Option .................................................................................................................................................... 4-12
Pulse Oximetry (SpO2) .... ... .... ... ... ... .................................................... ... ............................................................. 4-12
End Tidal Carbon Dioxide (EtCO2) ...................................................................................................................... 4-13
Noninvasive Blood Pressure ................................................................................................................................ 4-14
Ap p e n d i x A Overview ..........................................................................................................................................A-1
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E Series Service Manual

Preface

ZOLL® Medical Corporation’s E Series® Service Manual is intended for the service technician whose responsibility is to identify malfunctions and/or make repairs at the subassembly level. The ZOLL E Series Service Manual has five main sections and one appendix.
Preface—Contains safety warnings and an overview of the manual’s contents. Be sure to review this section thoroughly before attempting to use or service the E Series unit.
Chapter 1—Maintenance Tests explains how to check the defibrillator’s performance using a series of recommended checkout procedures to be conducted every six months.
Chapter 2—Troubleshooting provides a listing of the procedures and error messages to help the service technician detect faults and repair them. Chapter 3—Replacement Parts List displays a complete list of ZOLL part numbers for field replaceable parts available for the E Series unit, allowing
the service person to identify and order replacement parts from ZOLL.
Chapter 4—Functional Description provides technical descriptions for the E Series major subassembly modules. Appendix A—E Series interconnect diagrams and maintenance checklists.

Safety Considerations

The following section describes general warnings and safety considerations for operators and patients. Service technicians should review the safety considerations prior to servicing any equipment and read the manual carefully before attempting to disassemble the unit. Only qualified personnel should service the E Series unit.
Federal (U.S.A.) law restricts this unit for use by or on the order of a physician. Safety and effectiveness data submitted by ZOLL Medical Corporation to the Food and Drug Administration (FDA) under section 510(K) of the Medical
Device Act to obtain approval to market is based upon the use of ZOLL accessories such as disposable electrodes, patient cables and batteries. The use of external pacing/defibrillation electrodes and adapter units from sources other than ZOLL is not recommended. ZOLL makes no representations or warranties regarding the performa nce or ef fectivenes s of its product s when used in conjunction with pacing/d efibrillation elect rodes and adapter units fro m other sources. If unit failure is attributable to pacing/defibrillation electrodes or adapter units not manufactured by ZOLL, this may void ZOLL's warranty.
Only qualified personnel should disassemble the E Serie s unit.
WARNING! This unit can generate up to 2250 volts with sufficient current to cause lethal shocks.
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All persons near the equipment must be warned to STAND CLEAR prior to discharging the defibrillator. Do not discharge the unit’s internal energy more than three times in one minute or damage to the unit may result. Do not discharge a battery pack except in a ZOLL SurePower™
Charger Station or compatible ZOLL Battery Charging/Testing unit.
Do not use the E Series in the presence of flammable agents (such as gasoline), oxygen-rich atmospheres, or flammable anesthetic s. Using the un it near the site of a gasoline spill may cause an explosion.
Do not use the unit near or within puddles of water. Note: The E Series is protected against interference from radio frequency emissions typical of two-way radios and cellular phones (digital and analog)
used in emergency service/public safety activities. Users of the E Series should assess the unit’s performance in their typical environment of use for the possibility of radio frequency interference from high-power sources. Radio Frequency Interference (RFI) may be observed as shifts in monitor baseline, trace compression, or transient spikes on the display.

Additional Reference Material

In addition to this guide, there are several other components to the ZOLL E Series documentation. They include:
E Series Operator’s Guide - A comprehensive reference work that describes all the user tasks needed to operate the E Series.
E Series Configuration Guide - Describes the E Series features and functions whose operation can be customized by authorized users.
E Series Operator’s Guide Option Insert: 12-Lead ECG Monitoring- Describes using the 12-lead ECG monitoring option with the E Series un it.
E Series Operator’s Guide Option Insert: End Tidal Carbon Dioxide (EtCO
E Series Operator’s Guide Option Insert: Non-Invasive Blood Pressure (NIBP)- Describes using the NIBP option with the E Series unit.
E Series Operator’s Guide Option Insert: Pulse Oximetry (SpO
E Series Operator’s Guide Option Insert: Non-Interpretive 12-Lead ECG Monitoring- Describes using the non-interpretive 12-lead ECG monitoring
option with the E Series unit.
E Series Operator’s Guide Option Insert:12-Lead Reperfusion Therapy Algorithm - Describes the reperfusion therapy algorithm option for the E Series
)- Describes using the SpO2 option with the E Series unit.
2
unit.
)- Describes using the EtCO2 option with the E Series unit.
2

Conventions

WARNING! Warning statements describe conditions or actions that can result in personal injury or death.
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Caution Caution statements describe conditions or actions that can result in damage to the unit. Note: Notes contain additional information on using the defibrillator.

Service Policy Warranty

In North America: Consult your purchasing agreement for terms and conditions associated with your warranty. Outside of North America, consult ZOLL authorized representative.
In order to maintain this warranty, the instructions and procedures contained in this manual must be strictly followed. For additional information, please call the ZOLL Technical Service Department 1-800-348-9011 in North America.

Technical Service

If the ZOLL E Series unit requires service, contact the ZOLL Technical Service Department: Telephone: 1-978-421-9655; 1-800-348-9011 (US only) Fax 1-978-421-0010 Have the following information available for the Technical Service representative:
Unit serial number.
Description of the problem.
Department where equipment is used.
Sample chart recorder strips documenting the problem, if applicable.
Purchase Order to allow tracking of loan equipment.
Purchase Order for a unit with an expired warranty.
If the unit needs to be sent to ZOLL Medical Corporation, obtain a Service Request number from the Technical Service representative. Return the unit in its original container to:
ZOLL Medical Corporation 269 Mill Road Chelmsford, Massachusetts 01824-4105 Attn: Technical Service Department, SR #
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Technical Service for International Customers

International customers should return the unit in its original co ntainer to the nearest authorized ZOLL Medical Corporation Service Center. To locate an authorized service center, contact the International Sales Department at ZOLL Medical. See back cover of this manual.
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Chapter 1

Maintenance Tests

Overview

The E Series has two checkout procedures: the operator’s shift checklist and the extensive six-month maintenance tests checkout procedures. Because the E Series units must be maintained ready for immediate use, it is important for users to conduct the Operator’s Shift Checklist procedure at the
beginning of every shift. This proce dure c an be c omplet ed in a few mi nutes an d re quires no additional test equipment. (See the ZOLL E Guide for the Operator’s Shift Checklist.)
A qualified biomedical technician must perform a more thorough maintenance test checkout every six months to ensure that the functions of the E Series unit work properly. This chapter describes the step by step procedures for performing the six back of this document (ZOLL E
Series Maintenance Tests Checklist) to record your results of the maintenance tests.
month maintenance test checkout. Use the checklist at the
Series Operator’s
This chapter describes the following maintenance tests:
1. Physical Inspection of the Unit
2. Front Panel Button Test
3. 3, 5, and 12 Leads Test
4. Power Supply Test
5. Leakage Current Test
6. Paddles Test
7. Heart Rate Display Test
8. Calibrating Pulses on Strip Chart Test
9. Notch Filter Test
10. Heart Rate Alarm Test
11. Defibrillator Self Test
12. Synchronized Cardioversion Test
13. Shock Test
14. Summary Report Test
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15. Advisory Message Test
16. Pacer Test
17. SpO
18. EtCO
19. Barometric Pressure Calibration Chec k
20. CO2 Accuracy Check
21. NIBP Monitor Test
22. NIBP Volume Leak Test with Fluke Biomedi cal NIBP Analyzer
23. NIBP Volume Leak Test with Fluke Biomedical Cufflink NIBP Analyzer
24. NIBP Transducer Calibration Test
Monitor Test
2
Monitor Test
2

Before You Begin the Maintenance Tests

Assemble the tools or specialized testing equipment listed in the “Equipment You Need to Perform the Maintenance Tests” section shown below.
Keep an extra fully charged ZOLL E Series compatible battery available.
Schedule an hour to conduct the entire maintenance test.
Photocopy the checklist at the back of this document and use the copy to record your results. As you conduct each step of a procedure, mark the
Pass/Fail/NA check boxes on your checklist and then save it for your maintenance file.
Perform the tests in the order presented.
Perform all the steps of each test procedure.
Complete all the steps of the procedure before evaluating the test results.

Equipment You Need to Perform the Maintenance Tests

For testing purposes, you can substitute an equivalent device.
ZOLL Medical Electrode Adapter from Fluke Biomedical (part number 3010-0378).
Fluke Biomedical Impulse 4000 Defibrillator Analyzer with 1.06 software or higher.
Fluke Biomedical
ECG Simulator; 12 Lead Simulator for 12 Lead test (e.g., Symbio CS1201).
Stop watch.
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601 Pro Series International Safety Analyzer.
Standard series II PC flash memory cards.
PCMCIA card reader and PC.
RescueNet
Phillips #1 screwdriver.
Phillips #2 screwdriver.
Flatblade screwdriver.
Needle nose pliers without teeth.
Wooden cuticle sticks with bev eled edges (or similar non-conducting implements).
®
Code Review V3.31 or higher from ZOLL Data Systems.

Equipment You Need for the E Series Options Maintenance Tests

E Series Service Manual
Fluke Biomedical
SpO
EtCO
Paddles (if used).
Printer Paper.
Battery.
AC line cord.
3 lead, 5 lead and 12 lead ECG cables. (12 lead cable needed if 12 lead option is installed.)
Fluke Biomedical BP Pump NIBP Monitor Analyzer (For NIBP units only) with NIBP cable and cuff (if NIBP option is installed), or
Fluke Biomedical Cufflink Analyzer (if NIBP option is installed)
cable and sensor (if option is installed).
2
cable, and CAPNOSTAT 5 Mainstream cable with airway adapter, or CAPNOSTAT 5 Sidestream cable with cannula (if option is installed).
2
Index 2PFE SpO2 Simulator or equivalent. (For SpO2 units only.)
Note: The Fluke Biomedical BP Pump NIBP Monitor Analyzer and the Fluke Biomedical BP Pump NIBP Analyzer use different technologies for
testing NIBP monitors and therefore, the manual provides two di fferent procedures for performing the NIBP Volume Leak test with each of these types of test equipment.
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E Series Service Manual

1.0 Physical Inspection of the Unit

Tools Needed: None. Test Setup: None.
Observe this... Pass/Fail/NA
1.1 Housing Is the unit clean and undamaged?
1.2 Does the unit show signs of excessive wear?
1.3 Does the handle work properly?
1.4 Does the recorder door open and close properly?
1.5 Are input connectors clean and undamaged?
1.6 Are there any cracks in the housing?
1.7 Do the front panel or selector switches have any damage or cracks?
1.8 Are there any loose housing parts?
1.9 Paddles Do the adult and pedi plates have major scratches or show signs of damage?
1.10 Do the adult shoes slide on and off easily to expose the covered pedi plates?
1.1 1 Are the paddles clean (e.g., free of gel) and undamaged? (if applicable)
1.12 Cables Are all cables free of cracks, cuts, exposed or broken wires?
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1.13 Are all bend/strain reliefs undamaged and free of excessive cable wear?
1.14 Battery Is the ZOLL battery fully charged?
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Observe this... Pass/Fail/NA
E Series Service Manual
1.15 Is the battery seated in the battery well correctly?
Record your results on the Maintenance Test Checklist.
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2.0 Front Panel Button Test

Tools Needed: None. Test Setup:
1. Install strip chart paper into the recorder tray.
2. Install the battery in the unit or connect the A/C power cord to the unit and then plug the cord into an electrical outlet.
3. Connect the universal cable and ECG cable (3 lead, 5 lead, or 12 lead) to the ZOLL simulator, or Fluke Biomedical Impulse 4000 Analyzer (or
equivalent).
Do this... Observe this... Pass/Fail/NA
2.1 Turn the selector switch to MONITOR.
(For AED units, turn the selector switch to ON and select Manual mode.)
2.2 Press the LEAD button; three times for the 3
lead cable and seven times for the 5 lead cable.
2.3 Connect the 12 lead cable to unit and simulator.
Press the LEAD button and select the lead for each of the 12 lead settings.
2.4 Set the simulator to NSR of 120 BPM. To check
the size of the ECG waveform, press the SIZE button.
2.5 Press the ALARM SUSPEND button. Alarm symbol changes from disabled to enabled. If the alarm sounds, press
2.6 Press the RECORDER button. The strip chart paper moves out of the unit from the paper tray. Check that the
2.7 Open the paper compartment door.
Press RECORDER button.
Listen for 4 beep tones. PADS and MONITOR display on the monitor. NOTE: PADS is a factory default setting.
Each time you press the LEAD button, a different lead number appears under the LEAD heading on the display.
PADS, I, II, III will display a 3 lead ECG cable if connected or no ECG cable is connected.
PADS, I, II, III, AVR, AVL, AVF, V1 will display a 5 lead ECG cable. A 12 Lead cable will display PADS, I, II, III , AVR, A VL, AVF, VI, V2, V3, V4, V4,
V5, V6.
As you press the SIZE button five times (0.5, 1.0, 1.5, 2.0, 3.0), note that the size of the ECG waveform appropriately changes on the display.
the ALARM SUSPEND button to turn it off. The alarm will only be suspended for 90 seconds at this point. Press and hold the ALARM SUSPEND button for 3 seconds to disable alarms.
correct time, date, ECG lead annotation and waveform are recorded on the paper. (Set Time and Date, if necessary.)
CHECK RECORDER message appears on the monitor.
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E Series Service Manual
Do this... Observe this... Pass/Fail/NA
2.8 Close the paper compartment door. Press RECORDER button.
2.9 Press RECORDER button. Strip chart paper stops flowing out of paper tray.
2.10 Press the VOLUME softkey.
To increase the volume of the beep, press the Inc. softkey.
2.11 To decrease the volume of the beep, press the Dec. softkey.
2.12 Press the CONTRAST button. Contrast menu displays.
2.13 Press the CONTRAST button. To increase the contrast of the display, press
the Inc. softkey.
2.14 To decrease the contrast of the display, press the Dec. softkey.
Strip chart paper flows out of paper tray. Verify that the CHECK RECORDER message no longer displays.
The volume bar graph displays. Audible beep when the QRS wave displays. The bar graph increases on the
display indicating an increase in volume. This action does not increase the volume which is normal.
Note: The QRS tone is on or off. There is no gradual change in volume. If equipped, voice prompts are gradual. Note: The voice volume has 5 settings. Setting 3 is in the mid-range.
The bar graph decreases on the display indicating a decrease in volume. The volume shuts off at the last bar; otherwise, the volume is the same as originally set.
Background light and characters display. The contrast increases on the monitor display.
The bar graph increases on the display indicating an increase in contrast. The bar graph decreases on the display indicating a decrease in contrast. The
display contrast changes.
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2.15 Press the SUMMARY button. Summary menu displays on the monitor showing the summary report options.
2.16 Press the CODEMARKER button. Code marker menu displays.
2.17 Connect a/c current and install the battery. Turn the unit off.
9650-1450-01 Rev. A 1-7
The CHARGER ON indicator lights. The amber or green lights illuminate. Note: If both lights flash ON/OFF, the unit is defective or no battery is installed.
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E Series Service Manual
Do this... Observe this... Pass/Fail/NA
2.18 If applicable, connect d/c current and install the battery. Turn the unit off.
2.19 Remove the battery. Note that both charge lights (green and amber) flash alternately.
2.20 Replace the battery and the turn unit on. Note that the yellow charge light illuminates.
2.21 Press the ANALYZE button. The SELECT DEFIB MODE message appears on the monitor. (For manual
2.22 Move the selector switch to DEFIB. Select 2J. Press the CHARGE button.
2.23 Press and hold the ENERGY SELECT down arrow.
2.24 Press and release the ENERGY SELECT up arrow 19 times.
2.25 Press the CHARGE button. Note the display shows the unit charged up to 200J and the SHOCK button
2.26 Press the SHOCK button. The unit discharges and the SHOCK button is no longer lit. A 15 second strip
The CHARGER ON indicator lights. The amber or green lights illumi nate. The yellow light indicates the battery is being charged. The green light
indicates the battery is fully charged to present capacity. If both lights flash ON/OFF, the unit is defective or no battery is installed.
devices.) The display shows that the unit is charging. The SHOCK button lights when the
unit is charged. Ready tone for DEFIB sounds. Unit discharges internally and selected energy decrements to 1J.
1-10, 15, 20, 30, 50, 70, 85, 100, 120, 150, 200J.
lights.
chart automatically prints, displaying the number of joules delivered (if equipped with recorder and configured to print event).
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Record your results on the Maintenance Test Checklist.
1-8 9650-1450-01 Rev. A

3.0 3, 5, and 12 Leads Test

Tools Needed: 3 lead, 5 lead, and 12 lead cables. Test each cable separately. Test Setup:
1. The E Series unit must be config ured to displ ay ECG LEAD OFF message.
2. Connect the lead wires appropriate to each test to the Fluke Biomedical Impulse 4000 or equival en t (Symbio CS1201).
Do this... Observe this... Pass/Fail/NA
E Series Service Manual
3.1 Turn the selector switch to MONITOR. Select leads.
3.2 Disconnect one lead from the simulator. The ECG LEAD OFF message displays within 3 seconds (if configured).
3.3 Reconnect the lead. Repeat step 3.2 with the remaining leads.
3.4 Repeat 3.2 and 3.3 for 5 lead and 12 lead cables.
Record your results on the Maintenance Tests Checklist.
NO ECG LEADS OFF message displayed.
Wait for ECG LEAD OFF message to clear from the display (if configured).
NOTE: If heart rate alarm sounds, press and hold the ALARM SUSPEND button for 4 seconds to disable the alarms.
NOTE: When testing the 12 lead cable, the ECG LEAD OFF message displays when you pull off a limb lead. When you pull off a V lead, the ECG VX LEAD OFF message displays where “X” is the number between 1 and 6.
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E Series Service Manual

4.0 Power Supply Test (Optional)

Tools Needed:
2 red miniature alligator to miniature alligator leads.
1 black miniature alligator to miniature alligator test lead.
DC power supply (15 Amp minimum).
0.1Ω 1% resistor (¼W or greater).
1000Ω 1% ¼W resistor.
Fluke 75 multimeter or equivalent.
Test Setup:
1. Make sure the unit an d power supply are turned off.
2. Connect one end of the black lead to the “-” terminal in the battery well.
3. Connect the other end of the black lead to the “-” terminal of the power supply.
4. Connect the red lead to “+” terminal socket of the battery well. Use the middle pin with the plastic guard around it. Connect the other end of the red lead
to the “+” terminal of the power supply.
5. Set the power supply voltage to 7V.
Caution Be sure to connect the power supply properly to the E Series battery well terminals or damage to the unit may result. Do NOT raise the
power supply voltage above 12V.
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E Series Service Manual
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Do this... Observe this... Pass/Fail
4.1 Turn the selector switch to MONITOR. (For AED units, turn the selector switch to ON
and select Manual mode.)
4.2 Turn the unit off.
4.3 Adjust the power supply voltage to 10.3V and turn the selector switch to MONITOR (for AED units, turn the selector switch to ON).
4.4 Low Battery Test Set voltage to 9.9V.
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The unit should not turn on.
The unit should turn on.
No LOW BATTERY message displays.
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4.5 Set voltage to 9.4V. LOW BATTERY message displays within 30 seconds.
4.6 Shut Down Voltage Test Set voltage to 8.5V.
Record your results on the Maintenance Tests Checklist.
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Unit should shut off within 30 seconds.
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E Series Service Manual
Test Setup:
1. Remove red lead from power supply and connect to 0.1Ω resistor.
2. Connect other end of resistor to “+” terminal of power supply usi ng a second red lead.
3. Connect multimeter across the resistor.
4. Set voltage scale (if DVM is not autoranging) to 220 mV
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Do this... Observe this... Pass/Fail/NA
4.7 System Current Test Set power supply to 10.3V.
4.8 Turn the selector switch to MONITOR. (For AED units, turn the selector switch to ON
and select Manual mode.)
4.9 Turn unit off.
Record your results on the Maintenance Tests Checklist.
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Voltage across resistor should be 116 mV or less (< 1.16 A of ON current).
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Test Setup for Off Current Test:
1. Remove 0.1Ω resistor and replace with 1K Ω.
2. Connect DMM across resistor.
3. Set voltage scale to DCV.
4. Measure voltage across resistor.
Do this... Observe this... Pass/Fail
E Series Service Manual
4.10 Off Current Test Measure across resistor with unit turned off.
Record your results on the Maintenance Tests Checklist.
Voltage should be less than 450 mV (<450 μA of current).
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E Series Service Manual

5.0 Leakage Current Test

Tools Needed: See the manufacturer’s instructions or supplied specifications for the leakage tester you use. Test Setup: See the manufacturer’s instructions or supplied specifications for the leakage tester you use. Repeat leakage test with accessories: MFC,
external paddles, and anterior/posterior paddles.
Maximum Leakage Acceptance Limits
Normal Condition Single Fault Condition* ECG 10μΑ 50μΑ MFC 100μΑ 100μΑ Earth 500μΑ 1000μΑ
*Single fault considered AC mains on applied part.
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6.0 Paddles Test (If applicable)

Tools Needed: None. Test Setup: If applicable, connect the universal cable to the paddles and place the paddles in paddle wells.
Do this... Observe this... Pass/Fail/NA
E Series Service Manual
6.1 Turn the selector switch to DEFIB. Press and hold the ENERGY DOWN button on the sternum paddle.
6.2 Press and release the ENERGY UP button on the sternum paddle for each setting.
6.3 Press and release the RECORDER button on the sternum paddle.
6.4 Select 30J using the paddle ENERGY button. Press the CHARGE button on the Apex paddle.
6.5 Press and release the APEX SHOCK button. No discharge.
6.6 Press and release the STERNUM SHOCK button.
6.7 Press and hold both paddles SHOCK buttons. The unit discharges. The TEST OK message displays and the red LED turns
Record your results on the Maintenance Tests Checklist.
The energy selection decreases to 1J.
1-10, 15, 20, 30, 50, 70, 85, 100, 120, 150, 200J.
The recorder turns on. Press and release again to turn off.
The unit charges to 30J, then the red LED charge indicator illuminates and the charge tone sounds. (Note that the front panel shock button does not illuminate).
No discharge.
off. The recorder runs.
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E Series Service Manual

7.0 Heart Rate Display Test

Tools Needed:
Calibrated ECG simulator with 60Hz sine wave output capability.
Mini-phone plug for measuring output signal from 1 Volt ECG OUT jack (optional).
ECG Cable (3 or 5 leads).
Test Setup:
1. Turn the selector switch to MONITOR. Press LEAD button until “I” displays.
2. Connect the ECG leads to the Fluke Biomedical Impulse 4000 or equivalent.
3. Connect the ECG cable to the unit.
Do this... Observe this... Pass/Fail/NA
7.1 Set the ECG Simulator to 120BPM. The Heart Rate displays as 120 +/- 2 bpm
Record your results on the Maintenance Tests Checklist.
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8.0 Calibrating Pulses on Strip Chart Test

Tools Needed: None Test Setup: None.
Do this... Observe this... Pass/Fail/NA
8.1 Press the RECORDER button.
E Series Service Manual
8.2 Press and hold SIZE button to activate the calibration signal.
Record your results on the Maintenance Tests Checklist.
The strip chart displays a signal of 300 ppm with an amplitude of 10 mm +/- 1 mm. The signal also appears on the video display.
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9650-1450-01 Rev. A 1-17
E Series Service Manual

9.0 Notch Filter Test

Tools Needed: Fluke Biomedical Impulse 4000 (or equivalent). Test Setup:
1. Connect the ECG cable to the Fluke Biomedical Impulse 4000 or equivalent.
2. Connect the ECG cable to the unit.
Do this... Observe this... Pass/Fail/NA
9.1 Turn the selector switch to MONITOR mode. (For AED units, turn the selector switch to ON
and select Manual mode.)
9.2 Select lead I, size 3x. Select 60Hz (or 50 Hz for a 50Hz unit) on the
Fluke Biomedical Impulse 4000.
9.3 Press RECORDER button. Verify that the waveform amplitude on the strip chart is less than 1.5 mm.
9.4 Turn the ECG simulator off.
Record your results on the Maintenance Tests Checklist.
1-18 9650-1450-01 Rev. A
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10.0 Heart Rate Alarm Test

Tools Needed: Fluke Biomedical Impulse 4000
Do this... Observe this... Pass Fail/NA
E Series Service Manual
10.1 Turn the selector switch to MONITOR mode. (For AED units, turn the selector switch to ON
and select Manual mode.) Connect the ECG leads to the Fluke Biomedical
Impulse 4000. Set the simulator to 120 BPM and the defibrillator to lead II.
10.2 Press ALARMS. The alarm menu displays.
10.3 Press SELECT PARAM softkey until ECG HR displays.
10.4 Press INC> for state. Cursor scrolls through ENABLE, AUTO and DISABLE.
10.5 Press DEC>for state. Cursor scrolls through ENABLE, DISABLE, AND AUTO.
10.6 Press INC> until ENABLE displays. ENABLE displays.
10.7 Set LOW limit to 30, HIGH limit to 150 then, press the RETURN softkey.
10.8 Press ALARM SUSPEND button. No alarm sounds.
10.9 Remove a lead wire from the Fluke Biomedical Impulse 4000.
10.10 Reattach ECG Lead wire to Fluke Biomedical Impulse 4000 and hold the ALARM SUSPEND button on unit for 4 seconds.
10.11 Press the ALARM SUSPEND button. Alarm is enabled. Alarm symbol (without “X”) displays.
Lead II message displays. NSR ECG at 120 BPM +/- 2 displayed.
Cursor scrolls through parameters.
MONITOR displays.
The alarm symbol flashes and the heart symbol stops flashing. The ECG LEAD OFF alarm tone sounds. Recorder prints a stripchart showing a low heart rate, if enabled.
The alarm symbol has an “X through it. The heart symbol flashes with each QRS wave.
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10.12 Set simulator to 160 BPM or higher. Heart Rate Value is highlighted, alarm tone sounds, the alarm and the heart
symbol both flash.
10.13 Press the ALARM SUSPEND button in the unit. Alarm is suspended for 90 seconds. The alarm symbol has an “X” through it.
The heart symbol flashes with each QRS wave.
9650-1450-01 Rev. A 1-19
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E Series Service Manual
Do this... Observe this... Pass Fail/NA
10.14 Press and hold ALARM SUSPEND for 4 seconds to disable alarms.
Record your results on the Maintenance Tests Checklist.
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1-20 9650-1450-01 Rev. A
E Series Service Manual

11.0 Defibrillator Self Test

SHOCK HAZARD!
TAKE THE NECESSARY PRECAUTIONS TO GUARD AGAINST SHOCK OR INJURY BEFORE YOU START CONDUCTING THE DEFIBRILLATOR TESTS.
Keep hands and all other objects clear of the multi-function cable connections and defibrillator analyzer when discharging the defibrillator.
Before you discharge the defibrillator, warn everyone near the equipment to STAND CLEAR.
Caution Do NOT internally di scharge the unit more than 3 times in 1 minute. Note that multiple rapidly rep eatin g inte rnal discha r g es at more than
30 Joules may damage the unit.
Tools Needed:
MFC Test Port Connector 1004-0053-99 with universal cable.
MFC Test Adaptor Co nnector (Fluke Biomedical Part Number 3010-0378 or equivalent).
Fluke Biomedical Impulse 4000 or equivalent defibrillator analyzer.
ECG Cable.
Stop watch.
Test Setup:
1. Ensure the unit is turned off
2. Ensure the ECG cable is connected to the unit and analyzer.
Note: The universal cable should not be connected to any equipment at the beginning of this test.
Do this... Observe this... Pass/Fail
11.1 Turn the selector switch to DEFIB mode. (For AED units, turn the selector switch to ON
and select Manual mode.) Set leads to PADS.
9650-1450-01 Rev. A 1-21
CHECK PADS/POOR PAD CONTACT message displays.
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E Series Service Manual
Do this... Observe this... Pass/Fail
11.2 Connect the universal cable to the MFC test port.
11.3 Select energy level of 100J and press the CHARGE button.
11.4 Press the SHOCK button. Unit does not discharge. DEFIB PAD SHORT message displays.
11.5 Set energy level to 30J. Unit internally discharges.
11.6 Press the CHARGE butto n. Unit charges to 30J and displays DEFIB 30J READY. The charge ready tone
11.7 Press and hold SHOCK button. Unit discharges. TEST OK message and number of joules delivered message
Record your results on the Maintenance Tests Checklist.
DEFIB PAD SHORT message displays.
The charge time is >2 second and <10 seconds and SELECT 30J FOR TEST is displayed.
sounds.
displays. For example, using the message at the top of the printed strip chart would read as follows:
30 JOULES TEST OK. TEST_CUR=10-14A DEFIB_IMPED=0. The impedance value may range from 0 to 5Ω.
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1-22 9650-1450-01 Rev. A

12.0 Synchronized Cardioversion Test

Tools Needed: Fluke Biomedical Impulse 4000 or equivale nt defibrillator analyzer. Test Setup:
1. Connect the universal cable via the adapter (D.N.I #3010-0378) to the defibrillator analyzer.
2. Select cardioversion on analyzer. Input 1mV ECG signal at 60 -120 BPM.
Do this... Observe this... Pass/Fail
12.1 Press LEAD button to select PADS and Size X1.
E Series Service Manual
12.2 Press the SYNC softkey on the defibrillator. Enter synchronized cardioversion timing test mode on the defibrillator analyzer.
12.3 Select 200J.
12.4 Press the CHARGE button. When the SHOCK button lights, press and hold th e SHOCK button.
Record your results on the Maintenance Tests Checklist.
Sync appears on display. Sync markers display on the monitor. The sync marker appears as a down
arrow over the ECG R-wave peaks on strip chart and display.
Observe that the R-wave to shock delay (sync delay) is less than 60 milliseconds on the analyzer display.
Defibrillator discharges.
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9650-1450-01 Rev. A 1-23
E Series Service Manual

13.0 Shock Test

Tools Needed: Fluke Biomedical Impulse 4000 or equivalent defibrillator analyzer. Test Setup:
1. Stop watch.
2. Connect the universal cable via the adapter (D.N.I #3010-0378) to the defibrillator analyzer.
3. Ensure that a fully charged battery is installed in the unit.
Note: If your E Series AED does not have manual override capability, do not perform this test.
Do this... Observe this... Pass/Fail/NA
13.1 Turn the selector switch to DEFIB mode. (For AED units, turn the selector switch to ON
and select Manual mode.)
13.2 Press the ENERGY SELECT down arrow until 1J displays.
13.3 Press the CHARGE button.Wait for the SHOCK button to illuminate.
13.4 Press the SHOCK button. Unit discharges 0J-2J into the simulator. (Note: The displayed rhythm may
13.5 Repeat for all settings 1-200J Energy delivered is within + /- 15% or 2J of setting which ever is greater.
13.6 Press the ENERGY SELECT up arrow until 200J displays.
13.7 Press the CHARGE button and start timing with a stopwatch. Stop timing when the SHOCK button illuminates.
13.8 Press the SHOCK button. Record the value of the discharge energy that is
displayed on the analyzer.
DEFIB 1J SEL displays.
DEFIB 1J RDY displays.
change shape for 30 seconds before it returns to an original rhythm. This is caused by the operation of the adaptive bandwidth defibrillator recovery circuit.)
DEFIB 200J SEL displays.
Observe and record the value of the charge time on the stop watch. Charge time 3.0-6.0 sec.
200J discharge energy 170-230J.
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1-24 9650-1450-01 Rev. A
E Series Service Manual
Do this... Observe this... Pass/Fail/NA
13.9 Note the Patient Current and Defib Impedance on the strip chart.
13.10 (AED unit only) Disconnect the cable from the analyzer.
Record your results on the Maintenance Tests Checklist.
Patient Current 20-24A. Defib Impedance 46-54 Ohms.
CHECK PADS audio prompt.
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E Series Service Manual

14.0 Summary Report Test

Tools Needed: None. Test Setup:
1. Connect the universal cable to the defibrillator analyzer.
2. If you are using paddles, place the paddles on the analyzer’s discharge plates.
Do this... Observe this... Pass/Fail
14.1 Press and hold the SUMMARY softkey for 4 to 8 seconds to erase any previously stored data.
14.2 Set selector switch to DEFIB. Select 200J using the ENERGY SELECT button, and press the
CHARGE button. When charged, press the SHOCK button to discharge into the defibrillator
analyzer.
14.3 Wait 18 seconds, then press the Code Marker softkey. Press the CPR softkey.
14.4 Turn the unit off. Wait 10 seconds and then turn the unit on. Press the SUMMARY softkey, then press the PRINT CHART softkey.
Record your results on the Maintenance Tests Checklist.
ERASING REPORT displays.
The unit successfully discharges and prints a strip chart.
The Code Markers display.
Summary report prints. The report displays the correct date, time, the shock delivered and Code Marker event.
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1-26 9650-1450-01 Rev. A

15.0 Advisory Message Test

Tools Needed: None. Test Setup:
1. Connect the universal cable via the adapter (D.N.I #3010-0378).
2. Attach the E Series to the defibrillator analyzer.
Do this... Observe this... Pass/Fail
15.1 Connect universal cable to the simulator. Turn the selector switch to DEFIB mode. (For AED units, turn the selector switch to ON.)
E Series Service Manual
15.2 Select VF (ventricular fibrillation) on the simulator, then press the ANALYZE button.
15.3 Press the SHOCK button. Unit discharges.
15.4 Select the NSR (normal sinus rhythm) on the simulator, then press the ANALYZE button.
Record your results on the Maintenance Tests Checklist.
ANALYZING ECG message displays. STAND CLEAR message displays.* SHOCK ADVISED message displays.* PRESS SHOCK message displays*+
*AED’s audio prompts are standard. Advisory audio prompts are user configurable.
+If configured for auto charge.
ANALYZING ECG message. STAND CLEAR message.* NO SHOCK ADVISED message.*
*AED’s audio prompts are standard.
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9650-1450-01 Rev. A 1-27
E Series Service Manual

16.0 Pacer Test

Tools Needed: Fluke Biomedical Impulse 4000 Analyzer (software 1.06 or higher) with optional external plug in pacing module (TQA-17) or equivalent.
?
Note: The following tests are to be performed only on E Series units equipped with the optional pacing function. The pacer output can be measured using an oscilloscope set to DC coupling connected across a load resistor. (See diagram in column for universal cable
connector polarity.) The load resistor is a 100 ohm, 5 watt or greater. The pacer output is a positi ve going pul se, 40 +/- 2 ms durati on with an ampl itud e of
0.1 volt per milliamp of selected output (e.g., 40 milliamps of selected output has an amplitude of 4 +/- 0.5 volts the specified tolerance displayed on the oscilloscope).
If an external non-invasive pacer analyzer is being used, then follow the manufacturer’s guidelines for measuring the frequency (ppm), output (mA) and the pulse width measured in milliseconds. Note that the analyzer pace load resistor must be less than 250 ohms.
Test Setup:
1. Connect the universal cable from the E Series to the External Pacer Load (TQA-17) of the Impulse 4000.
2. Turn the Main Selector knob of the E Series to the Pacer mode.
Do this... Observe this... Pass/Fail
16.1 Set the PACER OUTPUT to 14 mA and disconnect MFC connector from the Fluke Biomedical Impulse 4000.
16.2
Reconnect the universal cable to the Fluke Biomedical Impulse 4000. Press Clear Pace Alarm softkey.
CHECK PADS and POOR PAD CONTACT message displays. The p ace alarm is active.
CHECK PADS and POOR PAD CONTACT message disappears. The pace alarm is cleared.
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16.3 Set rate to 180 ppm; output to 0mA. No output appears on the Fluke Biomedical Impulse 4000.
16.4 Increase the output to 20mA. Output on the Fluke Biomedical Impulse 4000 is 20mA +/- 5mA. Pulse width is
40mS +/-2mS.
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Do this... Observe this... Pass/Fail
16.5 Increase the output to 40mA. Output on the Fluke Biomedical Impulse 4000 is 40mA +/- 5 mA. Pulse width is 40mS +/-2mS.
16.6 Increase the output to 60mA. Output on the Fluke Biomedical Impulse 4000 is 60mA or +/- 5mA. Pulse width is 40mS +/-2mS.
16.7 Increase the output to 80mA Output on the Fluke Biomedical Impulse 4000 is 80mA or +/- 5mA. Pulse width is 40mS +/-2mS.
16.8 Increase the output to 100mA. Output on the Fluke Biomedical Impulse 4000 is 100mA or +/- 5mA. Pulse width is 40mS +/-2mS.
16.9 Increase the output to 120mA. Output on the Fluke Biomedical Impulse 4000 is 120mA or +/- 6mA. Pulse width is 40mS +/-2mS.
16.10 Increase the output to 140mA. Output on the Fluke Biomedical Impulse 4000 is 140mA or +/- 7mA. Pulse width is 40mS +/-2mS.
16.11 Decrease the output to 60mA.
Decrease the rate to 30 ppm.
16.12 Increase the rate to 40ppm. Pacer rate on Fluke Biomedical is 39-41 ppm.
16.13 Increase the rate to 60ppm. Pacer rate on is Fluke Biomedical is 59-61 ppm.
16.14 Increase the rate to 80ppm. Pacer rate on Fluke Biomedical is 78-82 ppm.
16.15 Increase the rate to 100ppm. Pacer rate on Fluke Biomedical is 98-102 ppm.
Pacer rate on Fluke Biomedical is 29-31 ppm.
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16.16 Increase the rate to 120ppm. Pacer rate on Fluke Biomedical is 118-122 ppm.
16.17 Increase the rate to 180ppm. Pacer rate on Fluke Biomedical is 177-183 ppm.
16.18 Decrease the rate to 50 ppm. Pacer rate on Fluke Biomedical is 49-51 ppm.
16.19 Connect the ECG cable to the E Series and
Fluke Biomedical Impulse 4000. Select the ECG at 60 BPM on the Fluke Biomedical Impulse 4000.
9650-1450-01 Rev. A 1-29
ECG at 60 BPM is seen on the display and no stimulus markers.
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E Series Service Manual
Do this... Observe this... Pass/Fail
16.20 Press the Async Pace softkey. ECG at 60 BPM seen on the display with the pace stimulus markers displayed. Async pace message displays.
16.21 Turn off Fluke Biomedical. Set Pacer Rate to
100ppm. Press the RECORDER ON button.
16.22 Press and hold 4:1 button. Observe the pace stimulus markers every 60 mm+/- 1.5 mm.
Record your results on the Maintenance Tests Checklist.
Observe the pace stimulus markers every 15mm +/-1mm.
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1-30 9650-1450-01 Rev. A

17.0 SpO2 Monitor Test for SpO2 Option

Tools Needed:
Masimo
Masimo
Fluke Biomedical Index 2PFE SpO
Test Setup:
1. Connect the universal cable to the MFC test plug.
2. DO NOT connect the ECG cable to the simulator.
3. Install the Masimo
4. Connect the Masimo
5. Place a fully charged battery into the battery well or connect to ac power (dc power, if equipped).
6. Ensure that the SpO
®
Reusable Sensor.
®
Patient Cable.
Simulator (or equivalent).
2
®
Patient Cable and attach the Masimo® sensor to the patient cable.
®
sensor to the finger simulation post.
Simulator is off.
2
Do this... Observe this... Pass/Fail
E Series Service Manual
17.1 Turn the selector switch to MONITOR. (For AED units, turn the selector switch to ON
and select Manual mode.)
17.2 Wait ten seconds. Turn on the SpO2 simulator. Press the SIM
softkey on the Index SpO2 Simulator. Press the MAN softkey.
17.3 Press the 02+ or 02- softkey of the simulator until the SpO2 output is at 98%.
17.4 Using the Index SpO2 Simulator, press the BPM+ or BPM- softkey until the heart rate is 230 BPM.
9650-1450-01 Rev. A 1-31
The SpO2 saturation percentage appears as a dashed line on the monitor.
The SpO2 PULSE SEARCH message displays.
The E Series SpO2 reading of 98 +/- 1% appears on the E Series monitor. Note that you may need to wait up to 2 minutes for the information to appear on the ZOLL display.
The SpO2 rate 230 BPM displays on the simulator screen. Note that you may need to wait up to 2 minutes for the information to appear on
the ZOLL display. The SpO2 saturation of 96-100% appears on the E Series display.
The heart
rate of 226-234 BPM displays on the E Series monitor.
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E Series Service Manual
Do this... Observe this... Pass/Fail
17.5 Using the Index SpO2 Simulator, press the BPM- softkey until the heart rate is 50 BPM
17.6 Using the Index SpO2 Simulator, press the 02+ softkey until the SpO
17.7 Press Wave 2 softkey. Select the SpO2 waveform.
17.8 Press RECORDER. The plethysmographic waveform prints on the strip chart paper.
17.9 Using the Index SpO2 Simulator, press the BPM- softkey until the heart rate is at 230 BPM.
17.10 Select Wave 2 SpO2. Verify that the waveform is displayed at the correct rate.
17.11
Record your results on the Maintenance Tests Checklist.
Remove the Masimo® patient cable.
output is at 72%.
2
The SpO The heart rate of 46-54 BPM displays on the E Series monitor.
The SpO The heart rate of 46-54 BPM displays on the E Series monitor.
Plethysmographic waveform appears on the ZOLL display.
The SpO The heart rate in the heart position of 226-2 34 BPM displays on the monitor.
Print the waveform.
saturation of 96-100% displays on the unit.
2
saturation of 70-74% displays on the unit.
2
saturation rate of 70-74% displays on the unit.
2
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1-32 9650-1450-01 Rev. A

18.0 EtCO2 Monitor Test (for EtCO2 Option)

Tools Needed: CAPNOSTAT 5 Mainstream cable with airway adapter, or CAPNOSTAT 5 Sidestream cable with cannula. Test Setup:
1. Install the battery.
Do this... Observe this... Pass/Fail
E Series Service Manual
18.1 Connect the CAPNOSTAT 5 CO2 Mainstream cable with airway adapter attached, or the CAPNOSTAT 5 Sidestream cable with the cannula attached, to the yellow connector at the back of the E Series.
18.2 Set the front panel switch to MONITOR or ON. For AED units, enter Manual Mode.
18.3 When the WARM UP message disappears, press the Param softkey, then select EtCO2 and press Enter.
18.4 Press the ZERO softkey, then wait for the ZERO DONE message.
18.5 Press the Return softkey.
18.6 Press the Wave 2 softkey until the CO2 waveform appears.
18.7 Breath normally into the airway adapter. A capnogram waveform appears.
Record your results on the Maintenance Tests Checklist.
NOTE: Make sure the airway adapter (for Mainstream), or the cannula (for Sidestream) is installed in the CO
WARM UP message appears on the display. NOTE: Warming up may take about 1 minute.
The ZERO DONE message appears.
A flat baseline CO2 waveform appears.
cable.
2
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9650-1450-01 Rev. A 1-33
E Series Service Manual

19.0Barometric Pressure Calibration Check

Tools Needed: None. Test Setup: None
Do this... Observe this... Pass/Fail/NA
19.1 Connect the CAPNOSTAT 5 CO2 Sensor to the yellow connector at the back of the E Series unit, and connect an airway adapter to the sensor.
19.2 While pressing and holding the second softkey from the left, turn the selector switch to Monitor (ON for AED units).
19.3 Wait for the sensor to warm up. The message WARM UP is displayed for approximately one minute.
19.4 Obtain the local barometric pressure in mmHg.*
19.5 Press the Baro Pr. softkey to enter the Barometric Pressure Calibration screen.
19.6 Use the Inc> and Dec< softkeys to set the second value on the pressure display line equal to your local barometric pressure.
19.7 Press the Return softkey to store the offset and return to the main EtCO2 Calibration screen.
Record your results on the Maintenance Test Checklist.
*The barometric pressure can be obtained from a calibrated barometer, or from the National Weather Service at www.nws.noaa.gov (enter your local zip code to get the local barometric pressure). Note that the barometric pressure is in inches of mercury, multiply it by 25.4 to convert to mmHg.
The unit displays EtCO2 Calibration screen.
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1-34 9650-1450-01 Rev. A

20.0CO2 Accuracy Check

Tools Needed: None. Test Setup: None
Do this... Observe this... Pass/Fail/NA
E Series Service Manual
20.1 Connect the CAPNOSTAT 5 CO2 Sensor to the yellow connector at the back of the E Series unit, and connect an airway adapter to the sensor.
20.2 While pressing and holding the second softkey from the left, turn the selector switch to Monitor (ON for AED units).
20.3 Wait for the sensor to warm up. The message WARM UP is displayed for approximately one minute.
20.4 Obtain current room temperature in Centigrade (Cº).
20.5 Press the Select Gas T emp softkey to enter the CO2 Accuracy screen
20.6 Use the Prev, Next, Inc and Dec softkeys to set each digit of the gas temperature parameter in the CAPNOST AT 5 CO2 Sensor until Gas
Degrees C is equal to the room temperature.
20.7 Press the Return softkey to store the temperature and return to the main EtCO2
Calibration screen.
20.8 Press the Zero softkey to zero the mainstream CAPNOSTAT 5 CO2 Sensor/Airway Adapter.
NOTE: Make sure the airway adapter (for Mainstream), or the cannula (for Sidestream) is installed in the CO2 cable.
The unit displays EtCO2 Calibration screen.
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20.9 Attach a regulated flowing gas mixture of 5%
, balance Nitrogen (N2) to the airway
CO
2
adapter (for Mainstream) or cannula (for Sidestream).
9650-1450-01 Rev. A 1-35
The gas flow rate should already be preset to 2 to 5 liters per minute.
E Series Service Manual
Do this... Observe this... Pass/Fail/NA
20.10 Set the Gas Balance settings of the CAPNOST AT 5 CO2 Sensor to that of the
calibration gas mixture (N The default gas balance is N2.
, N2O, or He).
2
20.11 Allow a few seconds for the gas mixture to stabilize and observe the CO2 Percent value.
20.12 1. Press the Return softkey to return to the
main EtCO2 Calibration screen.
Record your results on the Maintenance Test Checklist.
The calibration gas mixture and regulator are available from Respironics Novametrix. (Equivalent alternatives are available from other suppliers.)
• Gas Regulator: PN 6081-00
• Calibration Gas (carton of 4 tanks): PN 8964-00
The expected value is 5% ± 0.26%.
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21.0NIBP Monitor Test

The NIBP monitor test verifies the accuracy of the systolic, diastolic, and mean blood pressure measurements, as well as the pa ti en t p ulse rate calculation.
Tools Needed: Fluke Biomedical BP Pump NIBP Monitor Analyzer. Test Setup:
1. Connect the Analyzer’s simulator hose to the NIBP connector on the E Series unit.
2. Set the following parameters on the NIBP Analyzer:
Parameter Value
Systolic pressure 120 mmHg Diastolic pressure 80 mmHg Mean pressure 93 mmHg Heart pressure 80 bpm
Note: If you are using the Fluke® Biomedical CuffLink, you must change the shift value of the Blood Pressure Envelope to +3 on the Pressure Curve
Adjust Menu.
3. Make sure the ECG cable is not connected to the E Series unit.
4. If the SpO2 option is installed, make sure that the Masimo cable is NOT connected to the E Series unit.
Do this... Observe this... Pass/Fail
21.1 Turn the selector switch to MONITOR mode. (For AED units, turn the selector switch to ON
and select Manual mode.)
21.2 Ensure that the LEADS parameters is set to PADS (default).
If necessary, press the LEADS button to cycle through the values to select PADS.
21.3 Press the NIBP button on the E Series front panel
Verify that the values displayed are accurate within ±5 mmHg of the pressure parameters set on the NIBP Analyzer.
9650-1450-01 Rev. A 1-37
The E Series powers on in MONITOR mode.
The E Series displays PADS in the Lead selection field on the monitor.
The E Series initiates the blood pressure measurement cycle and displays the following measurements:
systolic pressure (115 - 125 mmHg)
diastolic pressure (75 - 85 mmHg)
mean pressure (88 - 98 mmHg)
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E Series Service Manual
Do this... Observe this... Pass/Fail
21.4 Press the SUMMARY button on the E Series front panel.
21.5 Select the Trend softkey, then select the NIBP Trend softkey.
Record your results on the Maintenance Tests Checklist.
The E Series displays a summary of the NIBP measurements, including the pulse rate reading (in the range of 77 - 83 bpm).
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E Series Service Manual

22.0NIBP Volume Leak Test with Fluke Biomedical NIBP Analyzer

The volume leak test verifies the integrity of the pneumatic system on the NIBP module. This test is optional at 6 months, but should be performed annually or every 10,000 readings, whichever comes first.
Tools Needed: Fluke Biomedical BP Pump NIBP Monitor Analyzer. Test Setup:
1. Connect the Analyzer’s simulator hose to the NIBP connector on the E Series unit.
2. Configure the NIBP Analyzer for the volume leak test. For example, on the Fluke Biomedical BP Pump:
Press the MODE button three times to go into Tests mode.
Press the SELECT button twice to access the volume leak test.
3. Make sure the ECG cable is not connected to the E Series unit.
4. If the SpO2 option is installed, make sure that the Masimo cable is NOT connected to the E Series unit.
Do this... Observe this... Pass/Fail
22.1 Turn the Selector Switch to OFF. After 10 seconds, press and hold the fourth
softkey from the left and turn the Selector Switch to MONITOR.
22.2 Press the Leak Test softkey. The E Series displays the NIBP Leak Test Screen.
22.3 On the NIBP Analyzer, set the pressure parameter to 200 mmHg.
22.4 On the E Series unit, press the Close Valves softkey.
9650-1450-01 Rev. A 1-39
The E Series powers on in the NIBP Service Mode.
The NIBP Analyzer displays a pressure reading of 200 mmHg.
The Valves status changes from OPEN to CLOSED.
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E Series Service Manual
Do this... Observe this... Pass/Fail
22.5 On the NIBP Analyzer, press the START TEST softkey.
Note: You must press the START TEST
softkey within 30 seconds of closing the valves on the E
22.6 On the NIBP Analyzer, press the STOP TEST softkey.
22.7 On the E Series unit, press the EXIT softkey twice.
Record your results on the Maintenance Tests Checklist.
Series unit.
After approximately 1 minutes, a number appears in the upper middle area of the NIBP Analyzer display.
If the Analyzer:
displays a Volume Leak reading <5, then the E Series unit has passed the test.
displays a Volume Leak reading >5, then the E Series unit has failed the test.
displays no Volume Leak reading, but maintains a stable pressure reading at or above 200 mmHg, then the E Series unit has passed the test; there is no volume leak.
In addition, the E Series displays the Analyzer’s pressure reading in the “Cuff Pressure” field.
After approximately 3 minutes, the valves on the E Series unit open. The NIBP Analyzer terminates the Volume Leak Test.
The E Series returns to the main NIBP Service Mode screen, then to normal Monitor mode operation.
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23.0NIBP Volume Leak Test with Fluke Biomedical Cufflink NIBP Analyzer

The volume leak test verifies the integrity of the pneumatic system on the NIBP module. This test is optional at 6 months, but should be performed annually or every 10,000 readings, whichever comes first.
Tools Needed: Fluke Biomedical/Fluke Biomedical Cufflink NIBP Analyzer. Test Setup:
1. Connect the Analyzer’s simulator hose to the NIBP connector on the E Series unit.
2. Connect the Analyzer to the E Series unit as described in the manufacturer’s instructions.
3. Configure the NIBP Analyzer for the volume leak test by selec ting Leak Test. Note that you can also consider using the internal Digi tal Manomete r and
stopwatch.
4. Make sure the ECG cable is not connected to the E Series unit.
5. If the SpO2 option is installed, make sure that the Masimo cable is NOT connected to the E Series unit.
Do this... Observe this... Pass/Fail
23.1 Turn the Selector Switch to OFF. After 10 seconds, press and hold the fourth
softkey from the left and turn the Selector Switch to MONITOR.
23.2 Press the Leak Test softkey. The E Series displays the NIBP Leak Test Screen.
23.3 On the NIBP Analyzer, set the pressure parameter to 200 mmHg.
23.4 On the E Series unit, press the Close Valves softkey.
9650-1450-01 Rev. A 1-41
The E Series powers on in the NIBP Service Mode.
The NIBP Analyzer displays a pressure reading of 200 mmHg.
The Valves status changes from OPEN to CLOSED.
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E Series Service Manual
Do this... Observe this... Pass/Fail
23.5 On the NIBP Analyzer, press the START TEST softkey.
Note: You must press the START TEST
softkey within 30 seconds of closing the valves on the E
23.6 On the NIBP Analyzer, press the F3 softkey. The NIBP Analyzer terminates the Volume Leak Test.
23.7 On the E Series unit, press the EXIT softkey twice.
Record your results on the Maintenance Tests Checklist.
Series unit.
After approximately 1 minutes, a number appears in the upper middle area of the NIBP Analyzer display.
If the Analyzer:
displays a Volume Leak reading <10, then the E Series unit has passed the test.
displays a Volume Leak reading >10, then the E Series unit has failed the test.
displays no Volume Leak reading, but maintains a stable pressure reading at or above 200 mmHg, then the E Series unit has passed the test; there is no volume leak.
In addition, the E Series displays the Analyzer’s pressure reading in the “Cuff Pressure” field.
After approximately 3 minutes, the valves on the E Series unit open.
The E Series returns to the main NIBP Service Mode screen, then to normal Monitor mode operation.
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24.0NIBP Transducer Calibration Test

The NIBP module’s pressure transducers are factory-calibrated prior to shipment. However, you can perform a two-point calibration procedure periodically to ensure accurate pressure measurements.
This procedure is optional at 6 months, but should be performed annually or every 10,000 readings, whichever comes first.
Tools Needed: Fluke Biomedical BP Pump NIBP Monitor Analyzer (or equivalent). Test Setup:
1. Connect the Analyzer’s simulator hose to the NIBP connector on the E Series unit.
2. Configure the NIBP Analyzer to simulate cuff pressure. For example, on the Fluke Biomedical BP Pump:
Press the MODE button three (3) times to go into Tests mode.
Press the SELECT button once to access the Pressure Simulator screen.
Note: These instructions apply to the Fluke Biomedical BP Pump; for equivalent devices, follow the manufacturer’s instructions.
3. Make sure the ECG cable is not connected to the E Series unit.
4. If the SpO2 option is installed, make sure that the Masimo cable is NOT connected to the E Series unit.
Do this... Observe this... Pass/Fail
24.1 Turn the Selector Switch to OFF. After 10 seconds, press and hold the fourth
softkey from the left and turn the Selector Switch to MONITOR.
24.2 Press the NIBP Calib softkey. The E Series displays the NIBP Transducer Calibration Screen.
24.3 On the NIBP Analyzer, set the pressure parameter to 0 mmHg.
24.4 On the E Series unit, press the Set Low softkey to calibrate the transducer to a 0 mmHg pressure reading.
24.5 On the NIBP Analyzer, set the pressure parameter to 250 mmHg.
9650-1450-01 Rev. A 1-43
The E Series powers on in the NIBP Service Mode.
The NIBP Analyzer displays a pressure reading of 0 mmHg.
The NIBP pressure transducer registers its voltage output at a known pressure of 0 mmHg. The field adjacent to the 0 mmHg value changes to PASS.
Note: If the E Series displays a FAIL reading, veri fy the NIBP Analyzer’s
pressure setting and connection to the E
The NIBP Analyzer displays a pressure reading of 250 mmHg.
Series and repeat the step.
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E Series Service Manual
Do this... Observe this... Pass/Fail
24.6 On the E Series unit, press the Set High softkey to calibrate the transducer to a 250 mmHg pressure reading.
24.7 On the NIBP Analyzer, set the pressure parameter to stimulate a different cuff pressure (for example, 205 mmHg).
24.8 On the E Series unit, press the Read Cuff softkey.
Verify that the value displayed is accurate within ±5 mmHg of the pressure parameter set on the NIBP Analyzer.
24.9 On the E Series unit, press the EXIT softkey twice.
24.10 Perform the NIBP Monitor Test (see “NIBP Monitor Test” on page 37) to verify functional operation of the NIBP option.
Record your results on the Maintenance Tests Checklist.
The NIBP pressure transducer registers its voltage output at a known pressure of 250 mmHg. The field adjacent to the 250 mmHg value changes to PASS.
Note: If the E Series disp lays a FAIL reading, verify the NIBP Analyzer’s
pressure setting and connection to the E Series and repeat the step.
The NIBP Analyzer displays the specified pressure reading.
The NIBP module measures the pressure from the NIBP Analyzer and displays the value in the Cuff Pressure field.
The E Series returns to the main NIBP Service Mode screen, then to normal Monitor mode operation.
The E Series passes all the criteria for the NIBP Monitor Test.
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War ning! NIBP transducer calibration can affect clinical readings of the NIBP parameter. Ensure that the NIBP Transducer Calibration
procedure is performed correctly, followed by an NIBP Monitor Test for verify proper operation.
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Chapter 2

T roubleshooting

Overview

This chapter describes the most common technical problems that biomedical technicians expe rience when checking the E Series during routine maintenance or when there is a malfunction of the unit. It also contains a list of error messages that users may see if the unit is not operating properly.
This chapter contains the following:
Troubleshooting tables for ECG Leads Off Messages and Monitor Displays
ZOLL E Series Error Messages
If the problems you encounter are not listed below, call ZOLL Medical Corporation’s Technical Service Department for further assistance. (See page vii for contact information.)
9650-1450-01 Rev. A 2-1
E Series Service Manual

T roubleshooting

The following tables show the most common troublesho oting issues and their solutions. First, attempt to solve the problem with “Recommended User Action.” If these steps do not solve the problem, follow the steps listed in the
“Recommended Technical Action” column.
Reported Problem Recommended User Action Recommended Technical Action
ECG LEAD OFF message displays.
(3, 5, 12 lead cable)
V LEADS OFF message displays.
Check preparation of ECG electrode site by cleaning the site, lightly abrading the patient’s skin and/or clipping the patient’s hair at the electrode site.
If electrode gels are dry, replace electrodes with new ones from a freshly opened package.
Verify that all leads are attached.
Set monitor to another lead.
Verify that the electrodes have not exceeded their expiration date.
If the user is not using V leads, attach V lead connector terminator
plug to the cable’s V lead connector.
If a V1 lead wire metal snap comes in contact with the patient’s skin, then the system will show all V leads as OFF.
Remove V1 leads and others away from the patient. Turn off the unit and wait ten seconds before turning it back on.
Try to reproduce the problem using a simulator.
Inspect the ECG cables looking for corrosion or
broken connector pins.
Check the cable for intermittent connections by flexing the cable at the yoke and snap connectors.
Check the cable connection to the defibrillator.
Inspect the ECG input connector and its pins.
Replace it, if necessary.
Inspect the ECG cable connection to the system board.
Inspect the system board ECG shielding.
Remove and replace the system board.
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Reported Problem Recommended User Action Recommended Technical Action
CHECK PADS/POOR PAD CONTACT message displays.
Flash or arcing under defibrillator pad.
Remove and reinsert PADS connector into the universal cable.
Check for damaged defibrillator pads, wires and or connector.
Check for dried out or expired defibrillator pads.
Clip (not shave) the patient’s hair and wipe pad contact area dry.
Connect the cable to the test plug. The DEFIB PAD SHORT
message displays to indicate that the cable is functioning properly.
If the DEFIB PAD SHORT message displays, then check the connections of the pads to the patient and to the defibrillator cable.
If the DEFIB PAD SHORT message does not display, remove the defibrillator from service.
Avoiding using alcohol and betadine in and around the treatment area because these skin preparations may lead to increased conductivity and/or bonding between the electrode’s adhesive and skin.
Check for gel droop. If the gel has leaked out of the gel treatment area, replace the electrode.
Ensure pads are coupling to the patient’s skin and connected to the universal cable.
Check for dried out gel on the defibrillator pad.
Clip patient’s excessive hair. Do not shave hair.
Check expiration date. Replace pad if date has expired.
Do not conduct chest compression through the pads because the
pads could be damaged leading to the possibility of arcing and skin burns.
Apply the back electrode first. If the front electrode is already in place when the patient is being maneuvered for placement on the back, the front may become partially lifted, possibly causing arching and skin burns.
Connect universal cable to the shorting plug. The DEFIB PAD SHORT message should display, when you SELECT PADS. If the message does not display, then:
Try another universal cable.
Check the cable from the universal cable
connector to the High Voltage Module.
Check the cable from the High Voltage Module to the system board.
Remove and replace the High Voltage Module.
Remove and replace the system board.
Call ZOLL Technical Support for assistance.
Ensure that wet gel pads are stored flat.
Displayed HR not accurate. No artifact present.
9650-1450-01 Rev. A 2-3
Verify heart rate flashes with each QRS on display.
Change lead selection.
Change ECG size.
Reposition ECG electrodes.
E Series Service Manual
Reported Problem Recommended User Action Recommended Technical Action
Displayed HR not accurate; artifact present.
False “Pacer Pulses Seen” The patient does not have an internal pacemaker, but pacer pulses are
Wandering baseline. See “Displayed HR not accurate.” above . Same as above example. Electronic interference. Check for possible excessive radio frequency interference.
Reduce or eliminate ECG artifact due to electrode or patient cable movement. Route cables so that they don’t pull on electrodes or swing excessively .
Ensure patient is motionless.
Check for possible excessive radio frequency interference.
Verify a good connection of electrodes to the patient.
Prepare the patient’s skin prior to the electrode attachment.
Move patient cables away from other electrical equipment,
especially any RFI source.
Ensure ECG cable fits snugly in unit.
Change ECG cable.
Replace/reposition ECG electrodes.
Disable “Enable Pacer Detection” to reduce the effect of artifact.
displayed.
Disable “Enable Pacer Detection” to reduce high frequency artifact.
Move patient cables away from other electrical equipment.
Check for contamination on snaps. Ensure springs are intact.
Check for intermittent ECG patient cable or connector wiring.
Replace ECG input connector.
Replace ECG connector to the system board
cable.
Replace system board.
Turn off sources of excessive RFI.
Move E Series unit away from RFI source.
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ZOLL E Series Error Messages

The following is a list of ZOLL E Series error messages that may appear on your display. The “User Advisory” column informs you about an action in progress or provides feedback on a user correctable situation that typically does not require further technical support. The “Technical Action” column describes what you as a technician can do to correct the situation. Note that these messages will sometimes overlap part of the waveform display.
First, attempt to clear the message by turning the Selector Switch to OFF fo r ten seconds, then back to the desired operating m ode. If the fault persists, call ZOLL Technical Service.
Error Message Explanation User
200J MAX BIPHASIC User attempted to set defibrillation energy >200J on
Biphasic Unit. No higher energy is available.
ANAL YSIS HALTED
AUDIO FAULT 136 Audio DSP hardware error. Replace audio board.
AUDIO NOT RECORDING Audio is not recording. AUDIO QUEUE FULL Indicates that the audio output queue is full. Additional
BATT HIGH CURRENT Battery is charged and battery current is >.1 A or:
BATT HIGH VOLTAGE Battery voltage > 15.5 v. Replace battery and or charger BATT LOW CURRENT Battery is not charged and battery current is <.35 A. Replace battery and or charger.
ECG analysis halted due to user interaction such as:
Lead/size change
Analyze button was pressed again
Impedance fault
Charging error detected in auto defib mode
voice prompts can't be queued at this time.
Battery is not charged and battery current is > 1.6 A.
Advisory
9
9
Technical Action
Replace system board.Turn unit off and back on again.
Install PCMCIA card. Replace system board. None.
Unplug from A/C. Remove the battery for 20 seconds. Reconnect all above. If the problem persists, replace battery and or charger.
BATT LOW VOLTAGE Battery voltage < 9.5 v. Replace battery and or charger. BATT OVERCHARGE Charger on for > 4 hours.
9650-1450-01 Rev. A 2-5
Replace battery and or charger.
E Series Service Manual
Error Message Explanation User
CABLE FAULT (Auto defib mode only.)
Incorrect A/D reading for paddle ID (similar to PADDLE FAULT).
CARD FULL Memory Card Full. CHECK CO2 SENSOR EtCO2 Sensor is unplugged or defective.
CHECK CO2 ADAPTER Airway adapter is removed, occluded or adapter zeroing
needs to be performed or was performed incorrectly.
CHECK PADS Message displayed in conjunction with either POOR PAD
CONTACT or DEFIB PAD SHORT.
CHECK PATIENT Background ECG analysis detects shockable rhythm. CHECK PULSE Alternate message for NO SHOCK ADVISED
message.Message also shown after delivering third shock when auto analyze 3 times option is enabled.
CHECK RECORDER Produced when paper tray is empty, paper jams or
recorder door is opened.
Advisory
9
9
9
9
9
9
9
9
Technical Action
Replace paddle set, universal cable and/or system board.
Check that sensor cable is plugged in and seated properly. Check that sensor is not exposed to excessive heat. If problem persists, replace the sensor.
Replace/Clean airway adapter. Zeroing performed automatically.
Ensure pads are coupled to patient. Check / replace pads and universal cable.
Replace system board.
Replace paper sensor board, system interconnect board, and/or system board.
CHECK SPO CLOCK FAULT 11 Real time clock oscillator failure. Replace system board. CLOCK FAULT 12 Real time clock back-up power supply failure. Found
CLOCK FAULT 13 One of the set time units (seconds, minutes, year, etc.) is
SENSOR Reposition SpO2 sensor on patient.
2
oscillator stopped at power-up, but oscillator now running when the system is running. (Oscillator only runs when main power is applied).
out of range.
Replace system board.
Replace system board.
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Error Message Explanation User
CONFIRM MANUAL MODE Displayed when manual mode is entered. Alerts user to
confirm that manual mode is desired.
DEFIB DISABLED User prompt issued simultaneously with other faults if
defib is disabled.
DEFIB FAULT 71 More than 50 internal dumps occurred in less than 20
minutes.
DEFIB FAULT 72 Charging inhibited, voltage out of range.
DEFIB FAULT 76 Capacitor voltage too high for selected energy. DEFIB FAULT 77 Capacitor voltage > than absolute rated max. Replace high voltage module or capacitor. DEFIB FAULT 78 Unable to charge defib cap. DEFIB FAULT 79 Defibrillator charging too slowly. Replace high voltage module or capacitor. DEFIB FAULT 80 4 defibrillator faults detected within 20 second period. Replace high voltage module or capacitor. DEFIB FAULT 81 Discharge switch in undefined state. DEFIB FAULT 84 “Upper” discharge transistor shorted (measured via
applicable A/D channel).
Advisory
9
Technical Action
Possible configuration problem. Replace high voltage module. Call ZOLL Technical Support.
Turn the unit to OFF and back on. If fault persists, replace high voltage module.
Turn the unit to OFF and back on. If fault persists, replace high voltage module.
Replace high voltage module or capacitor.
Replace high voltage module or capacitor.
Replace high voltage module or capacitor. Replace high voltage module.
DEFIB FAULT 85 “Lower” discharge transistor shorted (measured via
applicable A/D channel). DEFIB FAULT 86 One discharge switch closed during power up test. DEFIB FAULT 87 Both discharge switches closed during power up test. Replace paddles, control board or system board.
DEFIB FAULT 94 Processor fault causing safety monitor port to be non-
functional. DEFIB FAULT 95 Safe or shutdown line is not functional. Replace high voltage module. DEFIB FAULT 108 VMON voltage is less than the target energy during
charging.
9650-1450-01 Rev. A 2-7
Replace high voltage module.
Replace paddles, control board or system board.
Replace system board, high voltage module or capacitor.
Replace high voltage module or capacitor.
E Series Service Manual
Error Message Explanation User
DEFIB FAULT 109 Defib capacitor voltage is greater than selected energy
when defibrillator is charging or ready.
DEFIB FAULT 111 Defib capacitor voltage has exceeded the absolute
maximum acceptable voltage.
DEFIB FAULT 195 Current higher than expected was detected during the
Biphasic bridge test or immediately following a discharge.
DEFIB FAULT 196 Biphasic module not operating properly while charging.
DEFIB NOT CHARGED Discharge button is pressed but the unit is not charged.
Advisory
9
Technical Action
Replace high voltage module or capacitor.
Replace high voltage module, capacitor, and or system board.
Ensure pads/paddles are used properly.
Attempt to clear the message by turning the Selector switch to off then back to the desired operating modes.
Replace bridge or high voltage module. Charge again.
Attempt to clear the message by turning the Selector switch to OFF, then back to the desired operating mode.
Replace bridge or high voltage module.
DEFIB PAD SHORT Measured impedance between high voltage leads of MFC.
DISABLE SYNC Sync mode active when analyze pressed in defib. DISCHARGE FAULT Defib capacitor voltage is not decreasing. Replace high voltage module, capacitor, and/or
ECG FAULT 4 Communication fault between ECG processor and main
processor.
ECG FAULT 5 ECU RAM test failure, or ROM checksum test failure. Turn off unit and then turn on to reset. If fault
9
9
2-8
Ensure pads are coupled to patient. Check / replace pads or universal cable.
Replace system board.
system board. Turn off unit and then turn on to reset. If fault
persists, replace system board.
persists, replace system board.
9650-1450-01 Rev. A
E Series Service Manual
Error Message Explanation User
ECG LEAD OFF One or more ECG leads are not properly connected when
leads are selected as input. ECG TOO LARGE ECG signal too large for accurate shockable rhythm
analysis. ECG V LEAD OFF V LEAD cable is not properly attached. ECG V1 LEAD OFF Chest lead V1 is not properly attached to patient. ECG V2 LEAD OFF Chest lead V2 is not properly attached to patient.
ECG V3 LEAD OFF Chest lead V3 is not properly attached to patient.
ECG V4 LEAD OFF Chest lead V4 is not properly attached to patient.
ECG V5 LEAD OFF Chest lead V5 is not properly attached to patient.
ECG V6 LEAD OFF Chest lead V6 is not properly attached to patient.
Advisory
9
9
9
9
9
9
9
9
9
Technical Action
Check cable and patient connection. Change electrodes. Prepare patient’s skin.
Reduce ECG size.
Attach V LEAD cable. Reattach V lead. Check cable. Reattach V lead.
Check cable. Reattach V lead.
Check cable. Reattach V lead.
Check cable. Reattach V lead.
Check cable. Reattach V lead. Check cable.
ENTER ACCESS CODE Manual mode access code needed.
ERASING REPORT Summary report being erased. FAX BUSY FAX line at receiving FAX is busy. FAX DIALING Preparation for sending fax. FAX DONE Transmission complete. FAX PREPARING Preparing fax for transmission. FAX SENDING Transmitting fax.
9650-1450-01 Rev. A 2-9
9
9
9
9
9
9
9
Enter access code to enter manual mode with AED.
E Series Service Manual
Error Message Explanation User
INSERT CARD Check memory card
LOW BATTERY Low battery.
NO QRS DETECT Unit is in sync mode and heart rate is < 20 BPM or QRS
NO SHOCK ADV No shock advised. Advisory message when analysis finds
NOISY ECG Number of noisy analysis intervals exceeds threshold.
OPEN AIR DISCHARGE Cap voltage too high after discharge attempt, e.g., full
PACER DISABLED User prompt issued simultaneously with other pace faults
PACER FAULT 115 Flyback pulse width control circuit is not under proper
PACER FAULT 116 Failure to detect XPACE_ON.
No card installed in unit during manual or semi-automated modes.
amplitude is too low for proper synchronization.
non-shockable rhythm.
energy discharge did not occur.
if pacing is disabled.
control of the processor and gate array.
Advisory
9
9
9
9
9
Technical Action
Replace battery or plug into AC power. Replace charger.
Increase ECG size and/or change lead.
Stop all patient movement. Check connections. Press Analyze button again.
Replace paddles, and, or high voltage module and system board.
Replace high voltage module or system board.
Replace high voltage module, capacitor, or system board.
Replace high voltage module, capacitor, and/or system board.
PACER FAULT 117 Pace relay is stuck closed.
PACER FAULT 121 During pace, the pace pulse width <30ms or >50ms. PACER FAULT 122 Pace current is more than 15mA above and below
selected value.
PACER FAULT 123 Measured pace rate is too fast compared to selected rate. PACER FAULT 126 Issued in conjunction with message 122. Pace current is
more than 15mA and below selected value.
2-10
Replace high voltage module, capacitor, and/or system board.
Replace high voltage module, or system board. Replace high voltage module, or system board.
Replace high voltage module or system board. Replace high voltage module.
9650-1450-01 Rev. A
E Series Service Manual
Error Message Explanation User
PADDLE FAULT Cannot detect type of accessory attached to the universal
cable. PERFORM CPR Advisory message in AED auto defib mode.
POOR LEAD CONTACT One or more ECG leads are poorly connected or not
connected to patient. (User configurable.)
POOR PAD CONTACT Electrode impedance exceeds threshold.
PRESS ANALYZE Alternate message for check patient prompt. PRESS CHARGE Advisory message in conjunction with shock advised. PRESS SHOCK Prompt issued in AED auto defib mode when defib is
charged (ready). RECORDER FAULT 142 Strip chart system error. Check paper tray and paper path. Replace the
Advisory
9
9
9
9
9
9
Technical Action
Replace paddles, internal paddles, system board, high voltage module and/or universal cable.
Check electrode attachment to patient, cable connector to electrode, cable to unit connector. Broken unit.
Ensure pads are coupled to patient. Check / replace pads or universal cable.
Check impedance circuit calibration. Replace system board.
print head, system interconnect board and or the system board.
RECORDER FAULT 143 Strip chart failed power-up echo test. Communications
error.
RECORDER FAULT 147 Strip chart printhead over temperature. Check paper tray and paper path. Replace the
RELEASE BUTTONS Simultaneous external paddle button presses detected
before unit reached full defib charge (ready state). RELEASE SHOCK Discharge switch(es) closed when pressing charge button.
Discharge button pressed before defib reached ready
state.
9650-1450-01 Rev. A 2-11
9
9
Check paper tray and paper path. Replace the system interconnect board and/or the system board. Turn unit off and back on again.
print head, system interconnect board and/or the system board.
Release buttons.
Release shock button. Check paddles. Replace controls board.
E Series Service Manual
Error Message Explanation User
REPLACE BATTERY Battery voltage is less than absolute minimum. Shutdown
imminent.
REPLACE CARD Write errors during manual or semi-automated modes.
REPORT FULL Summary report memory full. REPORT HALTED Summary report stops printing unexpectedly. Turn unit off and then back on again. Print
SELECT 30J FOR TEST Attempt to run a self test at an energy other than 30J. SELECT DEFIB MODE Analyze button pressed in pace or monitor mode. SELECT LEADS 12 Lead monitor determined the user selected MFE.
SELECT LIMB LEADS Paddles or augmented ECG leads selected when
continuous analysis active or started.
SELECT PADS Lead I, II, or III selected when analyze pressed. SET CLOCK Real time clock failure: invalid date or time. Set date and time and/or replace system board.
Advisory
9
9
9
9
9
9
9
Technical Action
Replace with charged battery.
May have configuration card installed or write protection on.
Erase summary report.
Summary again. If fault persists, replace system board.
Select limb leads I, II, III or MFE
SET PACE mA Multiple copy errors are the product of intended software
or memory errors. If error reoccurs other than on entering pace the first time or after more than 10 minutes in other mode, the unit could be broken.
SET PACE RATE Multiple copy errors are the product of intended software
or memory errors. Multiple copies of pace rate don't match. If error persists, unit could be broken
SHOCK ADVISED Advisory message when analysis finds a shockable
rhythm.
SpO2 AMBIENT LIGHT Ambient light is too bright. Shield sensor from ambient light. Replace Sp0
9
9
9
2-12
Set pace current. If broken, replace system board.
Set pace rate. If broken, replace system board.
sensor. Replace Sp02 module
9650-1450-01 Rev. A
2
E Series Service Manual
Error Message Explanation User
SpO2 COMM ERR No transmissions from SpO2unit received. Communication
error or no communication from Sp0 SpO2 PULSE SEARCH Pulse search in progress.
STAND CLEAR (Auto defib mode only.) Single analysis mode just turned
on and defib idle. Patient rhythm is being analyzed. SYSTEM FAULT 1 No Watchdog. Turn off unit and then turn on to reset. If fault
SYSTEM FAULT 6 No communications received from ECU for 4 seconds.
SYSTEM FAULT 7 The A/D converter is not performing conversions in a
timely manner. SYSTEM FAUL T 36 PS_MON is out of range. Pace/defib is disabled as long as
condition exits. SYSTEM FAULT 37 Disable pace/defib and MFE monitoring. SYSTEM FAUL T 38 Failure to shutdown after “s hutdown order” is written to the
RTC. TEST FAILED MCU performed ipeak test (defib peak current) and unit
failed during 30J self test.
module.
2
Advisory
9
9
9
Technical Action
Replace Sp02 module and/or system board.
persists, replace system board. Turn off unit and then turn on to reset. If fault
persists, replace system board. Replace system board.
Replace system board.
Replace system board. Replace system board.
Replace universal cable, paddles or high voltage module, capacitor, or system board.
TEST OK MCU performed ipeak test (defib peak current) and unit
passed 30J self test. USE PADDLE DISCHG Front Panel discharge button is pressed when either
external paddles or internal spoons with discharge buttons
are connected. USE PADS (AUTO DEFIB MODE ONLY.)
Attempt to defib with paddles in auto defib (AED) mode.
Defib only allowed using PADS in AED modes. USE PADS TO PACE External paddles detected in pace mode.
9650-1450-01 Rev. A 2-13
9
9
9
9
E Series Service Manual
Error Message Explanation User
USER SETUP REQ Both copies of stored cal/config data are bad or have
never been programmed.
VF ALARMS OFF VF alarms disabled in pace mode or when paddles are
selected as leads.
VX LEADS OFF V lead not properly attached to patient. “X” denotes lead
number.
ZERO CO
ADAPTER New EtCO2 airway adapter needs to be zero calibrated.
2
Advisory
9
9
9
9
Technical Action
Perform configuration setup.
Reattach V lead.
Zero EtCO2 adapter.
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Chapter 3

Replacement Parts

This section contains a listing of the replacement parts available for the ZOLL E Series devices. Replacement parts may be ordered through an authorized ZOLL distribut or or directly from ZOLL Medi cal Corporation. Th e prices for parts are available
from ZOLL Medical Corporation’s Technical Service Department. When ordering parts, please provide the following information:
ZOLL E Series device model and serial number
Field Replaceable unit part number
Description of the replacement part
Description of problem
To order by mail from ZOLL Medical Corporation, address your request to:
ZOLL Medical Corporation 269 Mill Road Chelmsford, MA. 01824-4105 Attention: Technical Service Department 1-978-421-9655; 1-800-348-90 11; Fax: 1-978-421-0010
Note: ZOLL reserves the right to substitute different parts to reflect modifications and improvements in ZOLL E Series circuitry and design.
9650-1450-01 Rev. A 3-1
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Replacement Parts

Description Part Number
12-Lead Connector 1001-0232 Cable, AC Receptacle to AC Charger 9500-0739 Cable, Access Detect to ECG Out 7 POS 9500-0726 Cable, Battery Interconnect to AC Charger 9500-0717 Cable, Battery Interconnect to HV Module 9500-0718 Cable, Battery Interconnect to HV Module Defib 9500-0720 Cable, Battery Interconnect to HV Module Pace 9500-0719 Cable, Battery Interconnect to System Interconnect 9500-0721 Cable, Control to Display 9500-0712 Cable, Control to System I/O 9500-0713 Cable, Control to System Video 9500-0313 Cable, ECG Input 9500-0727 Cable, Flex, System to Isolated PS 20 POS 9500-0728 Cable, Ground Wire Assembly 9500-0302 Cable, Isolated Power Supply to ETCO2 20 POS 9500-0731 Cable, MFC Signal to HV Module 9500-0734 Cable, MS-11 PCB to SPO2 Connector 9500-0732 Cable, MS-11 to Isolated Power Supply 9500-0730 Cable, Paddle Harness 9500-0737 Cable, Ribbon Chart Card to Interconnect 9500-0736 Cable, Sensor to Printer Interconnect 9500-0729 Cable, Speaker 9500-0735
3-2
9650-1450-01 Rev. A
Description Part Number
Cable, SPO2 Module Assembly 1005-0160 Cable, System Interconnect to Communications Carrier 9500-0724 Cable, System Interconnect to NIBP 9500-0723 Cable, System Interconnect to PCMCIA 9500-0710 Cable, System Interconnect to Printer Interconnect 9500-0725 Cable, System to Battery Interconnect 51 POS 9500-0716 Cable, System to Biphasic DAC 20 POS 9500-0733 Cable, System to System Interconnect 51 POS 9500-0715 Cable, System to System Interconnect USB Interface 9500-0722 Connector Panel 9310-0905 Connector Panel Assembly No Options 1005-0013-01 Connector Panel Assembly with SPO2/ETCO2 1005-0013-02
E Series Service Manual
Connector Panel Assembly with SPO2/ETCO2/NIBP 1005-0013-03 Data Entry Membrane Switch 9170-0500 Display Assembly, Color LCD 1005-0009 ECG Connector Assembly 9301-0318 Handle, EMS 9310-0915 HV Capacitor 9126-0006 Knob, Main 9310-0521 Knob, Pacer 9310-0520 Left Rail 9310-0908 Lower Housing, EMS 9310-0900-90 NIBP Fitting 9330-0517
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E Series Service Manual
Description Part Number
Output ESD PCB Assembly 9301-0354 Paper Tray Out Sensor 9301-0385-01 PCMCIA Connector Assembly 3001-0300 Printer Frame 9310-0918 Printer Interconnect 9301-0387-01 Printer Leafspring 9320-0300 Printhead 0350-0350 Printhead Brush 9340-0102 Recorder Motor Assembly 3000-0100 Recorder Roller 9330-0300 Right Rail 9310-0907 Speaker Assembly 1005-0002 Upper Housing 9310-0902-90
3-4
9650-1450-01 Rev. A

Field Replacement Parts

Description Part Number
AC Charger PCB 9301-0388-01 AED Control Board with Pace 9301-0384-03 AED Control Board without Pace 9301-0384-04 Battery Interconnect 9301-0389-01 Bi-phasic Bridge 9301-0370-02 Bluetooth Module 3001-0 104 Communications PCB with GPS 9301-0390-01 Communications PCB with GPS And Bluetooth 9301-0390-02 Control Board with Audio, with Pace 9301-0384-07 Control Board with Audio, without Pace 9301-0384-08 Control Board with Pace 9301-0384-01
E Series Service Manual
Control Board without Pace 9301-0384-02 HV Module Assembly 1001-0278-02 Isolated Power Supply 9301-0383-01 Masimo SPO2 MS-11 PCB 3005-0001 NIBP Suntech Advantage 2 Assembly (Neonatal) 1001-0450 Printer Assembly 1005-0001 System Interconnect 9301-0381-01 System PCB 9301-0380-01
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Chapter 4

Functional Description

This chapter provides functional descriptions of the components contained in the ZOLL E Series and the E Series options. Refer to the interconnect diagram that delineates the different components of the defibrillator.
This chapter includes:
Main System Board
Main System Board Functions
Power Supply
User Interface
Audio I/O Module
ECG Front End
Multifunction (MFE) Paddles
Main CPU and EPU
High Voltage Modules
Defibrillator Charging and Discharging
High Voltage Capacitor Module
Pacer and Defibrillator Control Signals
Internal Discharge Resistor Module
AC/DC Charger
AC/DC Charger Module
System Interconnect Board
Stripchart Recorder
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E Series Service Manual
PCMCIA Slots
Front Panel and Display
E Series Options
12 Lead Monitoring
Pulse Oximetry (SpO
End Tidal Carbon Dioxide
Noninvasive Blood Pressure
2)
(EtCO
2)

Main System Board

The E Series electrical circuitry consists of several functional modules. Each module is physically located on one or more of the printed wiring board assemblies (PWBA). In some cases, a functional module is distributed across several assemblies within the unit. The main components of the E Series include:
Display
Main System Board
High Voltage Module
AC/DC Charger
Battery Interconnect Module
System Interconnect Module
High Voltage Capacitor
Some units are equipped with E Series options. These options include:
12 Lead ECG
Pulse Oximetry (SpO
End Tidal Carbon Dioxide (EtCO
Noninvasive Blood Pressure
)
2
)
2
4-2 9650-1450-01 Rev. A
Refer to the E Series Interconnect diagram to identify unit components described in this manual.
Module Location
Main Central Processing Unit (CPU) and ECU Main System PWBA Pacer/Defib Charging and High Voltage Control (Defib/Pace) High Voltage Module
Biphasic Bridge Module Internal Discharge Resistor HV Module AC or DC Power Supply/Battery Charger AC Charger PWBA
DC Charger PWBA
Main System PWBA ECG Front End Signal Acquisition Main System PWBA Battery Pack or Smart Battery Battery Interconnect PWBA User Interface and Controls Controls PWBA PCMCIA Interface System Interconnect, Main System Stripchart Recorder System Interconnect, Main System
E Series Service Manual
Audio I/O (optional) Main System PWBA
Audio Display PWBA
Controls PWBA SpO
(optional) Pulse Oximetry PWBA
2
Isolated Power Supply PWBA EtCO2 (optional) Isolated Power Supply PWBA
12 Lead (optional) Main System PWBA NIBP (optional) NIBP PWBA
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Main System Board Functions

The Main System Board contains th e major computing and control elements for the E Series unit. The printed wiring board assembl y (PWBA) receives signals from the front panel control switches, ECG input connectors and functional modules, such as the AC/DC charger, pacer/defibrillator modules, stripchart recorder and PCMCIA card interfaces, and if applicable, the SpO
these input signals to produce other signals that: 1) cont rol the operation of other modules within the system; 2) drive the unit’s front panel display and audio outputs and; 3) store data for retrieval via Summary Reports, PCMCIA cards and/ or a modem.
The electronic circuitry and software contained on the main system board performs the following major E Series functions:
1. Main CPU and memory.
2. ECG signal acquisition and processing for ECG leads including,
A/D conversion.
ECG signal filtering.
QRS detection.
Implanted pacemaker detection.
Heart Rate counting.
Shockable ECG rhythm analysis.
3. Data communications with and control over the SpO
4. Control over and safety monitoring of pacer and defibrillator functions performed by the High Voltage module and Biphasic Bridge module.
5. Physiological alarm processing.
6. Control switch monitoring for the front panel, accessory connec tion monitoring and cont ro l over th e system response to switch activation or accessory
, EtCO2 and NIBP modules.
2
connection to the E Series.
7. Format and updating of the front panel displ ay.
8. Primary power supplies for the unit.
9. Audio output generation and control (e.g., alarms, voice prompts, warning tones).
10.Audio signal processing, data compression and storage of voice recording data.
11. Real time clock and other time keeping functions.
12.Summary Report, 12 Lead ECG Reports data storage.
13.Monitoring of battery status and control over Battery Charging functions performed by the AC or DC Charger PWBA.
14.Data transmission to and control over the System Interconnect PCB functions, including the stripchart recorder and the PCMCIA slot functions.
, EtCO2 and NIBP modules. The Main System Board monitors and processes
2
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Power Supply

The power supply converts DC power from a removable battery or the AC/DC Battery Charger module to voltages required by the E Series hardware. The power supply circuit converts the raw battery or the Charger PWBA output voltages of +8.5 VDC to +16 VDC into the voltages shown in the table
below, including load and line regulation.
VOLTAGE DESCRIPTION VOLTAGE VDC
(Nominal)
FUSE_PWR Fused Input Power from Battery/Charger 12 SW_PWR Switched Input Power after Power Switch 12 3VDD + 3.3 VDC Power for Digital circuits 3.3 Switching @ 300 kHz 5VDD + 5.0 VDC Power for Digital circuits 5.0 Switching @ 300 kHz
-5VSS - 5.0 VDC Power for Analog circuits -5.0 Linear 12VEE + 12.0 VDC Power for Analog circuits 12.0 Linear 15VDD + 15.0 VDC Power for VPP and 12VEE 15.0 Switching @ 300 kHz LCD_BS LCD BIAS Power for LCD display - 18 Switching @ 100 kHz 3_3REF + 3.3 VDC Reference 3.3 Linear
COMMENTS
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ECG Front End

The ECG front end provides an electrically isolated serial interface between the main system board functions and patient interface ECG connectors. It performs the following:
Analog ECG amplification and signal cond itioning.
Pacemaker pulse detection.
ECG signals acquisition and analog to digital conversion.
ECG 3/5/12-lead detection.
ECG leads off detection.
Front-end defibrillator protection.
Isolated power conditioning.
Patient impedance measurement via MFE or paddles.

Multifunction Electrode (MFE)/PADS (System Board and High Voltage Module)

Selected for optimal performance for the application, a dedicated ECG amplifier with a limited bandwidth processes the signal. It is th en chopper modulated and coupled to the system sid e via an is olation transformer. On the system side, the signal is sy nchronou sly demodulated, converted by a 10 bit A/D at 250 samples per second and digitally processed by the main control unit of the system board.
To measure thoracic impedance, a high frequency (HF) measuring current passes through the patient’s chest and measures the resulting voltage across the electrodes. After amplification, the impeda nce si gnal i s synchron ously demo dulated. It is t hen co nverted to a stre am of pul ses with freq uency proportion al to the measured impedance.

CPU and EPU

The Main System Board contains two microprocessors. A Motorola HC-11 single chip microprocessor is used to acquire, convert and process ECG signals, (ECU). A Hitachi SH-3 RISC microprocessor acts as the system’s main CPU. The SH-3 CPU has an integrated on-chip multiplier, a cache memory , a memory management unit as well as data protection and virtual memory functions. It also has a timer, a real time clock, an interrupt controller, a serial communication interface (SCI), and other peripheral functions necessary for the system oper ation. The memory circuitry includes Flash ROM, internal flash non-volatile memory and DRAM.
The EPU acquires ECG data and runs the A/D convertor that sends data in the form of a serial stream to the CPU.
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High Voltage Module

The High Voltage (HV) module includes the high voltage circuitry required for pacing and defibrillation, including the defib charge circuitry, patient relay, safety relay, defib capacitor, defib choke and front end protection circuitry for the MFC ECG.
The following table describes the high voltage board components:
Component Function
Solid State Patient Relay Controls the delivery of therapeutic energy to patient. Safety Relay Discharges Defib capacitor into the internal discharge
resistor when defibrillator is not in use. Defibrillator Capacitor Stores energy for therapy. Defibrillator Choke Conditions waveform delivered to the patient.(DSW) Front End Protection Circuitry for
the MFC ECG
Protects ECG front end against defibrillator pulses.

Defibrillator Charging and Discharging

The defibrillator charges and discharges high voltage capacitor energy. A user can initiate a charge in three ways by 1) pressing the cha rge button on the front panel; or (2) pressing the charge button on the paddles; or (3) configuring unit to charge automatically when it detects a shockable rhythm following an ECG analysis. To initiate a discharge, a user depresses both shock buttons on the paddles or depresses a single shock button on the front panel.
The defibrillator circuit charges the high voltage capacitor to the energy level the user specifies.This circuit also provides feedback to the main system board on the high voltage capacitor's voltage level and discharges the high voltage capacitor energy through paddles or the universal cable. The defibrillator portion of the high voltage circuitry is active only when the front panel selector switch is set to DEFIB (or set to ON for AED units).
Charging
The charging process starts when the Main System Board detects a charge request. The defibrillator circuits begin charging the high voltage capacitor to the target voltage or energy that the user selects on the front panel display. The Main System Board continuously monitors the capacitor voltage signal to ensure that the high voltage capacitor charges at the proper rate. When the target voltage is reached, the Main System Board initiates a continuous beeper tone to indicate that defibrillator is ready to discharge. The target energy level displays on the display screen.
The defibrillator holds the energ y for 60 sec onds for manual un its and 15 seconds for AED units, refreshing the energy level as necessary. An intermitten t beep tone sounds during the last ten seconds (five seconds for AED unit) of the hold period. After the 60 second period, if the defibrillator has not been
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discharged, the ener gy is dissi pated i nto the in ternal discharge resistor by closing the safety relay (XSAFREL). The un it disc h arges internally and displays a warning message if it is not functioning properly.
Unlike previous ZOLL designs that isolated the patient from defib circuitry via an electromechanical patient relay, the E Series utilizes a bank of silicon­controlled rectifiers (SCRs). As the defibrillator capacitor is charged, the voltage is monitored via R1 - R4, which drive differential amplifiers referred to the system ground. These resistor dividers split the capacitor voltage more or less equally above and below ground in order that the positive capacitor terminal is approximately 1100 volts above ground, and the neg ative capacitor terminal is approximately 1100 volts below ground (at 200J setting). The voltage at the patient electrodes is set by the divider RN1 and RN2. These networks are each 5X 25 M (125 M total) whose total resistance is specified to be 125 M +\- 1%. As a result, the patient is nominally at ground and the hot switch bank is split into a ‘positive’ side and a ‘negative’ side.
Discharging
Initiating a discharge provides voltage to the patient relay and notification to the Main System Board through the PADMON signal. The Main System Board then controls activation of the patient relay. Energy delivered to the p atient goes through t he biphasic bridge/D AC assembly to create a defibrillat ion waveform. When the patient discharge SCRs are deactivated, the safety relay closes to internally dissipate any remaining energy.
If the E Series is in the self test mode, the energy is delivered internally. The microprocessor calculates the actual delivered energy from the current waveform and displays a TEST OK message on the display, if the self test meets the appropriate criteria. If the criteria are not met, a TEST FAILED message displays.

High Voltage Capacitor Monitor

Before charging the defibrillator, the High Voltage Capacitor monitor runs a self test to check the pace relay. The pace relay controls the high voltage circuitry configuration either for generating pace pulses or for charging the high voltage defibrillation capacitor.
The defibrillator capacitor is shunted for safety reasons with a resistor and relay to internally dissipate any energy remaining. When the Main System Board initiates a charge, this relay opens by providing a low level on signal XSAFREL. The safety relay is a biased reed switch. The relay is driven by Q318.
The pace relay driver is a grounded source switch Q308 that is biased on by R 593. It is hel d of f by Q330 when XPACEREL is '1' false. When XPACEREL comes true, Q330 is turned off, and Q308 is no longer clamped off.
The high voltage capacitor is charged by converting the system battery voltage to a pulsed high voltage by way of transformer T1. The basic operating frequency signal that is used to switch transistor Q1 providing current in the primary windings of the transformer T1 originates in the system board’s gate array.
When the high voltage capacitor is charging, the Main System Board independently monitors the capacitor voltage through signal VMON. If the Main System Board detects an improper level, it halts operation by setting SAFE high. This disables the SCR discharge circuitry and flyback transformer drive.
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The patient relay discharges via the signal PATREL_DRV generated by XPATREL and Q304, Q323, and Q322. PATREL_DRV is disabled when XPACE_SEL is at a logic low.
When the patient relay activation completes, the Main System Board releases the XPATREL signal. Several hundred milliseconds later, the safety relay closes to ensure the high voltage capacitor energy is completely dissipated.
The Pacer circuit produces and delivers user-controllable pace pulses to the pacing electrodes. To initiate pacing, the front panel switch is turned to PACER and the OUTPUT and RATE controls are set. Pacing current amplitude is constant during the pulse and is determined by the positio n of the front panel PACER OUTPUT dial. Pacing pulse rate is determined by the position of the front pan el PACER RA TE dial. The paci ng pulse d uration is fixed at 40 milliseconds.

Pacer/Defibrillator Control Signals

The Pacer/Defibrillator Control charges the high voltage capacitor to a voltage requested by the main system board in response to user energy selections. It delivers defibrillator energy to the patient through the patient connector to the paddles and pacer electrodes or multi-function electrodes (PADS). This control also generates pacing pulses at rates and amplitudes requested by the main system board in response to user selections, controls biphasic waveform defibrillation, and measures pace current and high voltage capacitor voltage by two independent channels.
The following signals control the operation of the Pacer/Defibrillator subsystem:
Analog Voltage Operation Comment
VCAP Anal og voltage spanning 0 - 2.5 V for 0 - 5000V capacitor voltage. Used by the defib charging controller. VMON Analog voltage spanning 0 - 2.5 V for 0 - 5000V capacitor voltage. Used by the defib monitor. VSNS Pace duty cycle voltage, scaled as 0 - 2.5 V for 0 - 100% duty cycle. When multiplied by the pulse width (as read from PW_READ)
battery voltage is proportional to the actual pace current. VCTL Analog control voltage scaled 0 - 2.5 V for pace current of 0 - 140 ma. Onl y active in pace mode. FET_MON Analog voltage monitors the condition of the discharge transistors. Provides a signature voltage in case of a fault. PAT_CUR Bound on the range of 0 - 2.5 V and accommodates defib currents of -
50 to +100 A
9650-1450-01 Rev. A 4-9
Analog signal representing the patient current during a defib
discharge.
E Series Service Manual
Logic Control Signal Operation
XPWR_ENABLE This logic signal from the gate array enables the charging circuit when true, and inhibits the charging circuit when false. SAFE This logic control signal is generated by the Main System Board to halt the pace/defib function in the event of a detected fault. SHUTDOWN
XPACE_ON This logic signal is generated by an optocoupler, and indicates that the pace output circuit is active. It is '0' true when pace
XSAFREL Logic signal from the GA that operates the safety relay when '0' true. XPACEREL Logic signal from the GA that operates the pace relay when '0' true. XP ATREL: Logic signal from the GA that operates the solid
XPAT_ENABLE Logic signal from the processor controlled by the monitor that grants operation of the solid state patient relay. It is false during
XPACE_SEL Hardware only signal from the front panel switch that is at '0' during pace. Used as an additional safety interlock on the solid
This logic signal is true during reset and fault conditions. (VCC error, watchdog error, etc.) and generator.
current is flowing.
state patient relay when '0' true.
pacing.
state patient relay so that operation of the relay during pacing is additionally disabled.
halts operation of the PD

Internal Discharge Resistor Module

The Internal Discharge Resistor Module contains the internal discharge resistor, and a means for dissipating the heat generated by the internal discharge.

AC/DC Charger Module

The AC/DC Power/Battery Charger provides a universal (IEC 320) connection to the AC mains or to a DC source, input line filtering and double-pole fusing (for a mains input), AC-DC and DC-DC conversion and isolation barrier between the E power necessary to run the E Series in any mode of operation, as well as providing additional charging current to the battery. When the E Series is turned off but connected to an external AC or DC source, the charger module controls battery charging currents and voltages needed to charge the E Series battery. These voltages and currents are controlled in response to the main CPU signals that manage the battery charging process.
Series and power sources. This module also provides the
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System Interconnect Module

The system interconnect PWBA receives signals from the Main System Board and in turn controls operation of the stripchart recorder and PCMCIA functions.

Stripchart Recorder

The Stripchart Recorder module includes a microprocessor, serial interface to the main system board and circuitry which drive the stripchart recorder’s motor and printhead in response to the main CPU signals. Based upon signals sent by the main CPU, the recorder’s main processor drives the recorder stripchart motor, formats data for printing on the chart and drives the printhead. It also detects when the sensor drawer is not properly fitted into the unit, when the paper supply is out and needs to be refilled and the print head temperature.

PCMCIA Slots

The PCMCIA interface module supports two PCMCIA slots which accept Type I and/or Type II PCMCIA cards. These cards may be read or written to. Data sent by the main CPU is passed to the installed PCMCIA card via the system interconnect PWBA.

Front Panel and Controls PWBA

The User Interface Module provides several functions th at enable the user to operate the unit. The user interface has a display monitor and three rotary selector switches. One selector switch is for three modes: pacer, monitor and defibrillation. The two other knobs are for pacer output and pacer rate. The unit interface also has specific buttons for defibrillation, including the ENERGY SELECT button, the CHARGE button, the ANALYZE button and the SHOCK button. The five softkeys underneath the display provide specific operations depending on the unit’s configuration. The other push buttons (from left to right) are used for volume control, monitor illumination, summary report, and code markers. The CHARGER ON indicator displays the status of the unit’s power supply.
This input module on the front panel and the Main System Board provides a beeper for the AC/DC Power/Battery Charger. The Controls PWBA is physically located in the front panel assembly. Units that are equipped for voice recording include a microphone and audio signal
conditioning circuitry on the Controls PWBA.

Isolated Power Supply Module

The Isolated Power Supply Module provides electrically isolated power to the EtCO2 and SpO2 modules. It also provides the electrically isolated serial communications and isolated control signals between the EtCO
9650-1450-01 Rev. A 4-11
and SpO2 modules and the main system PWBA.
2
E Series Service Manual

E Series Options

The following sections describe the E Series options.

12 Lead Option

The ZOLL E Series 12 lead option is used to ac qu ire ECG d ata needed to assist in the diagnosis of myocardial infarction (“heart attack”), often caused by a coronary artery occlusion. The 12 lead ECG can be viewed on the display one lead at a time in monitoring and diagnostic bandwidths and printed in the standard 4x3 format with 12 simultaneously acquired leads.
The 12 lead option provides for the recording, printing and automated analysis of 12 lead ECG using GE Marquette 12SL™ Analysis and supports the transmission of these reports by fax to a remote locat ion, such as a hospital. In t he pre-hospital en vironment, the 12 lead rep orts can be faxed to a physician as the patient is en route to the Emer gency De partment . As a result, t he physici an can ini tiate hospita l accommodati ons immediately, such as ac tivating the staff of the cardiac catheteriz ation lab, prior to the pa tient’s arrival and subsequent treatment. Or the patient may be treate d in the pre-hospital environment with thrombolytic agents.
The 12 lead cable is required to produce 12 lead reports. E Series unit must have the 12 lea d option installed. All limb leads and V-leads must be connected to initiate a 12 lead acquisition. Printed 12 Lead bandwidth is use r configurable to be ei ther 0.05-150 Hz (per AAMI EC1 1) or 0.05-40 Hz. The 0.05 -40 Hz bandwidth selection is used to reduce noise art ifact in t he h ig h end of the diagnostic frequency range. Reports can be printed in a standard 4x3 or Cabrera format. Faxed reports can be configured in a 2x6 format in addition to 4x3 and Cabrera formats.
The GE Marquette 12SL Analysis algorithm provides measurements of the 12 lead waveforms along with interpretive statements. The algorithm is interpretive, not “diagnostic.” (A physician should always confirm interpretive statements. A diagnosis requires a complete clinical assessment including other modalities, such as a physical examination.) 12SL produces global waveform measurements as well as a measurement matrix containing measurements on each lead. Both the interpretive statements and measurement matrix are configurable to be printed or not printed.
The acquired 12 lead with 12SL may be faxed to a remote location using landline or cellular phone technology. Specific PCMCIA fax modems are supported and the modem determines the specific phone compatibility. The E Series supports Group 3 facsimile, Class 1, Class 2 and Class 2.0. 12 lead reports may be re-printed or re-transmitted using the Patient Records capability. Individual patient records may be selected based on patient ID, date, and time.

Pulse Oximetry (SPO2)

The ZOLL E Series pulse oximetry option enables the user to continuously, noninvasively, and painlessly monitor the percentage of oxygen saturation of arterial hemoglobin at a peripheral measurement site (i.e. foot, toe or finger.)
The oximetry sensor contains two light emitting diodes, or LEDs, that transmit red and infrared light through the body’s extremities. A photodetector receives the transmitted light. Oxyg en saturat ed bloo d absorbs light d if ferently than u nsaturated b lood. Th us the a mount of red and infrared light absorbed
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by the blood flowing through a suitable peripheral area of the body, such as the finger in adults and the foot in neonates, can be used to calculate the ratio of oxygenated hemoglobin to total hemoglobin in the arterial blood. The monitor displays this ratio as percent SpO
Normal values typically range from
2.
95% to 100% at sea level. The E Series uses a Masimo® Pulse Oximetry Circuit Board which features a fundamentally distinct method of acquiring, processi ng and reporting arteria l
oxygen saturation and pulse rate. The E Series’ SpO
module (Masimo® Circuit Board) connects to the Masimo sensors and reports monitoring results
2
(oxygen saturation, pulse rate, pulse waveform, etc.) via a serial digital interface to the E Series system board. The E Series system provides isolated DC power and serial communication to the SpO
Board via the Isolated Power Supply board.
2

End Tidal Carbon Dioxide (EtCO2)

The ZOLL E Series EtCO2 option continually and noninvasively monitors the patient’s carbon dioxide in respiratory gases and from these measurements computes End Tidal CO In addition, the unit can configure an alarm to sound when the unit detects EtCO set by the user. This option is intended for use in all critical monitoring environments including ventilato r sup p ort, patient transport, and anesthesia and is
intended for monitoring all patient types, including adu lt, pediatric, and neonatal. E Series units equipped with software revision 2.00.000 or higher support two End Tidal Carbon Dioxide (EtCO2) monitoring options for the continuous
measurement of respiratory carbon dioxide (CO interchangeably.
and respiration rate. The unit can display and prin t a recordin g of EtCO2 readings, respiration rates, and capnograph waveforms.
2
values and respiration rates that are above or below accept able ranges as
2
) and respiration rate. These options use the same connector on the E Series unit and may be used
2
The first option uses a unique, mainstream, solid-state, infrared sensor called the CAPNOSTAT® 5 Mainstream CO2 Sensor. The CAPNOSTAT 5 CO2 sensor is attached to an airway adapter that connects to an endotracheal (ET) tube or other airway and measures gases flowing through these breathing circuit components. A disposable mouthpiece may be connecte d to the adapt er for moni toring non-intu bated pat ients. A CAPNO for use with non-intubated patients. This option provides for O
delivery while monitoring expired CO2.
2
mask™ is also available
2
The second option is a sidestream sampling system called the LoFlo™ CO2 Module. The LoFlo module contains a gas sampling pump, which draws sma ll samples of gas from the patient’s airway via a nasal/oral cannula or airway adapter, and passes these gases through a solid state infrared sensor (located away from the patient’ s airway) that mea sures CO
. While the sidestream system is typica lly used on non-in tubated patients, it can also be used fo r EtCO2
2
measurement on intubated infant, pediatric and adult patients. The sidestream system should not be used, however, on patients who cannot tolerate the 50ml/min removal of the sample gases from their breathing circuit. The sidestream module uses specially designed cannulas and airway adapters for sampling airway gases and passing them through an integrated sample cell, which connects to the LoFlo module ’s CO
sensor. These cannulas inc orporate
2
a filter and sample cell, providing maximum filtration of fluids and contaminants, and protecting the system from aspiration of these fluids. In both systems, the CO2 sensor generates infrared light and beams it thro ugh the airway adapt er or sample cell to a detec tor on the opposite sid e. CO2 from
the patient, flowing through the mainstream airway adapter or sample cell, absorbs some of this infrared energy. The E
Series unit determines CO2
concentration in the breathing gases by measuring the amount of light absorbed by gases flowing through the airway or sample cell.
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The E Series unit displays EtCO2 (the concentration of carbon dioxide detected at the end of each exhalation) as a numerical value in millimeters of mercury (mmHg), percent (%), or kilopascals (kPa). In addition, the unit can display a capnogram. This capnogram is a valuable clinical tool that can be used to assess patient airway integrity and proper endotracheal (ET) tube placement. The unit calculates respiration rate by measuring the time interval between detected peaks of the CO2 waveform. The technology differentiates between waveforms caused by breathing and those caused by ca rd io gen i c oscillations and artifact.

Noninvasive Blood Pressure

The Non-Invasive Blood Pressure (NIBP) option on the E Series unit allows you to take a single blood pressure measurement, STAT measurements (automatically repeated measurements over a 5 minute period), or automatic measurements at repeating pre-selected intervals.
The ZOLL E Series NIBP option is indicated for the non-invasive measurement of arterial blood pressure for resting patients in critical care and transport. The NIBP option is designed to measure blood pressure for adult and pediatric patients.
The patient blood pressure cuff and hose connect to the E Series unit through the NIBP connector on the rear panel of the unit. The NIBP button on the front panel of the E softkeys on the NIBP menu.
The NIBP module measures the oscillometric pulses transmitted throu gh the blood pressure cuf f and hose, and ca lculates the bloo d pressure measurements accordingly. The blood pressure information (including the patient’s systolic, diastolic and mean blood pressure values) is shown on the E
Series allows you to initiate and terminate blood pressure measurements. You can also initiate and terminate measurements using the
Series monitor.
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E Series Service Manual
Appendix A
Overview
This appendix includes:
Interconnect Diagram for the E Series Unit
ZOLL E Series Maintenance Tests Checklist
Photocopy the checklists and use the copies to record the results of the maintenance tests performed on the E Series equipment; keep them for your records.
9650-1450-01 Rev. A A-1
E Series Service Manual
AC Receptacle
*
Earth ground post
*
MFE Connector/Patient
ETCO2 Connector
9500-0731
9500-
MS-11
0730
Assembly
1005-0160
*
*
9301-0388-01 AC Charger
9500-0718
1001-0278-02 HV Module
*
9301-0370-02 Bipha sic Bridge /DA C
9301-0383-01 Isolated Power Suppl y
9500-0719
9500-0720
9500-0734
*
Capacitor
9500-0716
9500-0733-50
9500-0728-50
9500-0721
9301-0389-01 Battery Interconnect
9500-0716-50
9301-0380-01 System
9500-0715-50
9500-0722
1005-0002
9500-0713-50
9500-0313
9500-0715-50
Speaker
9500-0712
9301-0384-01 Controls
Membrane Keypad
9500-0727-50
9500-0726
Display
9500-0312
1001-0345
9500-0519 1001-XXXX
Microphone
ECG Input Connector
Access Detect ECG Out/RS232 Conne ct or
SPO2 Connector
* - integrated assembly ** - assembly integration planned
PCMCIA C age
9301-0390-01 Communications
9500-0710
9500­0724
NIBP Assemb ly
9301-0381-01 System Interconnect
9500-0723-50
**
Hose
9500-0725
9301-0387-01 Printe r I nterco nn ect
*
Printer Motor
9500-0736 9500-0729
P r int He ad
9301-0385-01 Paper/Recorder Sensors
Rev 0.01
Figure 1: Interconnect Diagra m for E Series Unit
A-2 9650-1450-01 Rev. A
ZOLL E Series Maintenance Test Checklist
Serial No. Location Tester Signature Date
Result of Check:
o No action required o Minor problems corrected o Disposable supplies
replaced
o Major problems identified
(unit out of service)
Additional Remarks
1.0 Physical Inspection 2.0 Front Panel Button
Pass Fail N/A
1.1
1.2
1.3
1.4
1.5
1.6
1.7
1.8
1.9
1.10
1.11
1.12
1.13
1.14
1.15
o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o
Test
Pass Fail N/A
2.1
2.2
2.3s
2.4
2.5
2.6
2.7
2.8
2.9
2.10
2.11
2.12
2.13
2.13a
2.13b
2.14
2.15
2.16
2.17
2.18
2.19
2.20
2.21
2.22
2.23
2.24
2.25
o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o
2.26
o o o
3.0 Leads Test
Pass Fail N/A
3.1
o o o
3.2
o o o
3.3
o o o
3.4
o o o
4.0 Power Supply Test
Pass Fail N/A
4.1
o o o
4.3
o o o
4.4
o o o
4.5
o o o
4.6
o o o
4.8
o o o
4.10
o o o
5.0 Leakage Current Test
Pass Fail N/A
5.1
o o o
6.0 Paddles Test
Pass Fail N/A
6.1
o o o
6.2
o o o
6.3
o o o
6.4
o o o
6.5
o o o
6.6
o o o
6.7
o o o
7.0 Heart Rate Display Test
Pass Fail N/A
7.1
o o o
8.0 Pulse Calibra tion Test
Pass Fail N/A
8.2
o o o
9.0 Notch Filter Test
Pass Fail N/A
9.3
o o o
10.0 Heart Rate Alarm Test
Pass Fail N/A
10.1
o o o
10.2
o o o
10.3
o o o
10.4
o o o
10.5
o o o
10.6
o o o
10.7
o o o
10.8
o o o
10.9
o o o
10.10
o o o
10.11
o o o
10.12
o o o
10.13
o o o
10.14
o o o
11.0 Defibrillator Self Test
Pass Fail N/A
11.1
o o o
11.2
o o o
11.3
o o o
11.4
o o o
11.5
o o o
11.6
o o o
11.7
o o o
12.0 Synchronized Cardioversion Test
Pass Fail N/A
12.2
o o o
12.4
o o o
13.0 Shock Test
Pass Fail N/A
13.2
o o o
13.3
o o o
13.4
o o o
13.5
o o o
13.6
o o o
13.7
o o o
13.8
o o o
13.9
o o o
13.10
o o o
9650-1450-01 Rev. A A-3
ZOLL E Series Maintenance Test Checklist
Serial No. Location Tester Signature Date
14.0 Summary Report Test
Pass Fail N/A
14.1
o o o
14.2
o o o
14.3
o o o
14.4
o o o
15.0 Advisory Message Test
Pass Fail N/A
15.2
o o o
15.3
o o o
15.4
o o o
16.0 Pacer Test 17.0 SpO
Pass Fail N/A
16.1
16.2
16.3
16.4
16.5
16.6
16.7
16.8
16.9
16.10
16.11
16.12
16.13
16.14
16.15
16.16
16.17
16.18
16.19
16.20
16.21
16.22
o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o
17.1
17.2
17.3
17.4
17.5
17.6
17.7
17.8
17.9
17.10
18.0 EtCO
18.2
18.4
18.6
18.7
19.0 Barometric Pressure Calibrationt
19.7
20.0 CO
20.7
20.8
20.11
Monitor Test
2
Pass Fail N/A
o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o
Monitor Test
2
Pass Fail N/A
o o o o o o o o o o o o
Pass Fail N/A
o o o
Accuracy Test
2
Pass Fail N/A
o o o o o o o o o
21.0 NIBP Monitor Test
Pass Fail N/A
21.2
o o o
21.3
o o o
21.5
o o o
22.0 NIBP Volume Leak Test with Bio-Tek NIBP Analyzer
Pass Fail N/A
22.4
o o o
22.5
o o o
22.6
o o o
23.0 NIBP Volume Leak Test with Fluke Biomedical Cufflink NIBP Analyzer
Pass Fail N/A
23.4
o o o
23.5
o o o
23.6
o o o
24.0 NIBP Transducer Calibration
Pass Fail N/A
24.4
o o o
24.6
o o o
24.8
o o o
24.9
o o o
24.10
o o o
9650-1450-01 Rev. A A-4
E Series Service Manual

Index

Numerics
200J MAX BIPHASIC message 2-5 2PFE SpO2 Simulator 1-3
A
AC or DC Power Supply 4-3 AC/DC Charger module 4-10 Advisory message test 1-27
ANALYSIS HALTED message 2-5 AUDIO FAULT 136 message 2-5
Audio I/O 4-3
AUDIO NOT RECORDING message 2-5 AUDIO QUEUE FULL message 2-5
B
BATT HIGH CURRENT message 2-5 BATT LOW CURRENT message 2-5 BATT LOW VOLTAGE message 2-5 BATT OVERCHARGE message 2-5
Battery Pack 4-3
C
CABLE FAULT message 2-6 CHECK PADS/POOR PAD CONTACT message 2-3 CHECK PULSE message 2-6 CHECK RECORDER message 2-6 CHECK SPO2 SENSOR message 2-6 CLOCK FAULT 11 message 2-6 CLOCK FAULT 12 message 2-6 CLOCK FAULT 13 message 2-6 CONFIRM MANUAL MODE message 2-7
Contacting Technical Service vii Conventions vi
D
Defib Capacitor 4-7
DEFIB DISABLED message 2-7 DEFIB FAULT 108 message 2-7 DEFIB FAULT 109 message 2-8 DEFIB FAULT 111 message 2-8 DEFIB FAULT 71 message 2-7 DEFIB FAULT 72 message 2-7 DEFIB FAULT 76 message 2-7 DEFIB FAULT 77 message 2-7 DEFIB FAULT 78 message 2-7 DEFIB FAULT 79 message 2-7 DEFIB FAULT 80 message 2-7 DEFIB FAULT 81 message 2-7 DEFIB FAULT 84 message 2-7 DEFIB FAULT 85 message 2-7 DEFIB FAULT 86 message 2-7 DEFIB FAULT 87 message 2-7 DEFIB FAULT 94 message 2-7 DEFIB NOT CHARGED message 2-8 DEFIB PAD SHORT 2-3 DEFIB PAD SHORT message 2-8
Defibrillator
charging and discharging
energy levels 4-7 Defibrillator Choke 4-7 Defibrillator self test 1-21
DISABLE SYNC message 2-8 DISCHARGE FAULT message 2-8
Discharging 4-8
E
E Series
description
main components 4-2
ECG FAULT 4 message 2-8 ECG FAULT 5 message 2-8
ECG Front End 4-6 ECG Front End Signal Acquisition 4-3
ECG LEAD OFF message 2-9 ECG LEADS OFF message 2-2
4-1
4-7
ECG TOO LARGE message 2-9 ECG V LEADS OFF message 2-9 ECG V2 LEAD OFF message 2-9 ECG V3 LEAD OFF message 2-9 ECG V4 LEAD OFF message 2-9 ECG V5 LEAD OFF message 2-9 ECG V6 LEAD OFF message 2-9 ENTER ACCESS CODE message 2-9
Equipment You Need for the Maintenance Tests
Testing Equipment
ERASING REPORT message 2-9 Error Message
ANALYSIS HALTED AUDIO FAULT 136 2-5 AUDIO NOT RECORDING 2-5 BATT HIGH CURRENT 2-5 BATT OVERCHARGE 2-5 CABLE FAULT 2-6 CHECK RECORDER 2-6 CLOCK FAULT 12 2-6 CLOCK FAULT 13 2-6 CONFIRM MANUAL MODE 2-7 DEFIB DISABLED 2-7 DEFIB FAULT 108 2-7 DEFIB FAULT 109 2-8 DEFIB FAULT 111 2-8 DEFIB FAULT 71 2-7 DEFIB FAULT 72 2-7 DEFIB FAULT 76 2-7 DEFIB FAULT 77 2-7 DEFIB FAULT 78 2-7 DEFIB FAULT 79 2-7 DEFIB FAULT 80 2-7 DEFIB FAULT 81 2-7 DEFIB FAULT 84 2-7 DEFIB FAULT 85 2-7 DEFIB FAULT 86 2-7 DEFIB FAULT 87 2-7 DEFIB FAULT 94 2-7 DEFIB FAULT 95 2-7 DEFIB NOT CHARGED 2-8 DEFIB PAD SHORT 2-8 DISABLE SYNC 2-8
1-2
2-5
IN-1
E Series Service Manual
DISCHARGE FAULT 2-8 ECG FAULT 5 2-8 ECG LEAD OFF 2-9 ECG TOO LARGE 2-9 ECG V2 LEAD OFF 2-9 ECG V3 LEAD OFF 2-9 ECG V4 LEAD OFF 2-9 ECG V6 LEAD OFF 2-9 ENTER ACCESS CODE 2-9 ERASING REPORT 2-9 FAX DIALING 2-9 FAX DONE 2-9 FAX PREPARING 2-9 FAX SENDING 2-9 INSERT CARD 2-10 LOW BATTERY 2-10 NO QRS DETECT 2-10
EtCO2
Isolated Power Supply Assembly
4-11
EtCO2 Isolated Power Supply Assembly 4-3
F
FAX DIALING message 2-9 FAX DONE message 2-9 FAX PREPARING message 2-9 FAX SENDING message 2-9
Front End Protection Circuitry
High Voltage Module
G
4-7
Gel droop 2-3
H
High Voltage Capacitor monitor 4-8 High Voltage Module Assembly 4-7
I
INSERT CARD message 2-10 Interference
radio and cell phone
vi
Internal Discharge Resistor Module 4-10
Components of Charge 4-10
Isolated Power Supply
function
L
4-11
Logic Control Signal 4-10 LOW BATTERY message 2-10
M
Main System Board 4-3 Maintenance Tests
equipment
1-3
Messages 2-3 Monitoring
User interface module
N
4-11
NO QRS DETECT message 2-10 NO SHOCK AD message 2-10 NOISY ECG message 2-10
Notch filter test 1-18
O
Ordering Replacement Parts
part numbers
P
3-5
Pacer Defibrillator function 4-9 PACER OUTPUT knob
pacing
4-9
PCMCIA Interface 4-3
Power Supply
MCU
4-5
Power supply
function
R
4-5
Radio frequency emissions vi Radio Frequency Interference vi
S
Safety Consideration v Safety Relay 4-7 Safety Warnings v SELECT 30J FOR TEST message 2-12 SELECT DEFIB MODE message 2-12 SELECT LIMB LEADS message 2-12 SELECT PADS message 2-12 Service
Address
vii
Service Policy Warranty vii
United States
Outsideof the United States
vii
SET CLOCK message 2-12 SET PACE RATE message 2-12 SHOCK ADVISED message 2-12 Solid State Patient Relay
High Voltage Module
4-7
SpO2 Isolated Power Supply Assembly
4-3
STAND CLEAR 2-13 Storing pads 2-3 Strip Chart Recorder 4-3 SYSTEM FAULT 2 message 2-13 SYSTEM FAULT 6 message 2-13 SYSTEM FAULT 7 message 2-13
IN-2
E Series Service Manual
T
Technical Service Department
Address
3-1
Test
3, 5, and 12 Leads
1-9
Advisory Message 1-27 Calibrating Pulses on Strip Chart 1-17 Check Summary Report 1-26 Defibrillator Self Test 1-21 EtCO2 Monitor 1-33 Front Panel Button 1-6 Heart Rate Alarm 1-19 Heart Rate Display 1-16 Leakage Current 1-14 Notch Filter 1-18 Pacer 1-28 Paddles 1-15 Power Supply 1-10 Shock 1-24 SpO2 Monitor 1-31 Synchronized Cardioversion 1-23
Troubleshooting
Displayed HR not accurate
2-4
Electronic interference 2-4 Wandering baseline 2-4
Z
ZERO CO2 ADAPTER message 2-14 ZOLL E Series Text Messages 2-2 ZOLL Medical Corporation
Address
Ordering parts for E Series
3-1
Service request number vii
ZOLL Technical Service Department vii
Fax number vii Telephone numb er vii
U
User Interface Module 4-11
V
V LEADS OFF Messages 2-2 Voltage
Power supply
W
4-5
Warnings v
IN-3
E Series Service Manual
IN-4
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